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FearLess in Cognitively Intact Patients With Glioma (FearLess)

Ashlee Loughan, PhD - ashlee.loughan@vcuhealth.org

NCT05604365
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Inclusion Criteria:
Patient inclusion:
• Confirmed glioma diagnosis (grade II-IV) via histopathology
• Be a minimum of 2 weeks post surgical repair or biopsy (if applicable)
• Elevated FCR [> 13 on Fear of Cancer Recurrence Inventory]
• Primarily English speaking Caregiver Inclusion:
• Loved one, or non-paid care partner to a patient with a confirmed glioma diagnosis (grade II-IV) via histopathology
• Elevated FCR [> 13 on Fear of Cancer Recurrence Inventory]
• Primarily English speaking
• Age 18+
Exclusion Criteria:
Patient:
• Cognitive impairment [< or equal to 31 on the Telephone Interview for Cognitive Status (TICS)]
• Inability to attend virtual sessions (e.g. due to lack of stable internet connection, difficulty using technology)
• Inability to understand and provide informed consent. Caregiver:
• Inability to attend virtual sessions (e.g. due to lack of stable internet connection, difficulty using technology)
• Inability to understand and provide informed consent.
Behavioral: FearLess Intervention
Glioma, Fear of Cancer
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Virginia Commonwealth University Richmond, Virginia Ashlee Loughan, PhD - (ashlee.loughan@vcuhealth.org) Autumn Lanoy - (lanoyeam@vcu.edu)

Salad Bars in the National School Lunch Program: Impact on Dietary Consumption Patterns in Elementary School Students

Sarah M Farthing, MS - sarah.malone@vcuhealth.org

NCT05605483
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Inclusion Criteria:
Students • All K-6th grade students at target schools who participate in the school lunch program on rating day Cafeteria staff • All cafeteria personnel at the randomly selected target schools will be eligible to complete surveys
Exclusion Criteria:
Students • Unsure sex of child Cafeteria staff • None
Other: Salad bar, Other: Waitlisted control
Diet, Food, and Nutrition
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Healthy Lifestyles Center at the Children's Hospital of Richmond at VCU Henrico, Virginia Sarah M Farthing, MS - (sarah.malone@vcuhealth.org) Melanie K Bean, PhD - (melanie.bean@vcuhealth.org)

Study of Tecovirimat for Human Monkeypox Virus (STOMP)

ACTG Clinicaltrials.gov Coordinator - ACTGCT.gov@fstrf.org

NCT05534984
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Inclusion Criteria (All participants; Arms A, B, and C):
• Laboratory-confirmed or presumptive HMPXV infection.
• HMPXV illness of <14 days duration immediately prior to study entry.
• At least one active (not yet scabbed) skin lesion, mouth lesion, or proctitis with or without visible ulcers.
• Non-pregnant people of reproductive potential must agree to use at least one effective means of contraception when engaging in sexual activities that can result in pregnancy, from the time of enrollment through the end of study participation. Additional Inclusion Criteria for Arms A and B:
• Age ≥18 years at the time of study entry Additional Inclusion Criteria for Arm C; Participants who meet the above entry criteria who also meet any of the following criteria will be registered to Arm C:
• Participants age <18 years at the time of study entry
• Those with severe HMPXV disease Those with or without severe disease and with one or more of the following will also be enrolled into Arm C:
• Severe immunosuppression
• Skin conditions placing the person at higher risk for disseminated infection Exclusion Criteria (All participants; Arms A, B, and C):
• Prior or concomitant receipt of tecovirimat (e.g., under an alternative access mechanism.
• Planned initiation of intramuscular cabotegravir/rilpivirine during study drug administration or for two weeks following completion of study drug administration. Participants who are stable on long-acting intramuscular cabotegravir/rilpivirine may enroll.
• Participants who, in the judgement of the investigator, will be at significantly increased risk as a result of participation in the study.
• Participants who require intravenous dosing of tecovirimat.
Drug: Tecovirimat Oral Capsule, Drug: Placebo, Drug: Tecovirimat Oral Capsule (Open Label)
Monkeypox
HMPXV
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Study Locations

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Alabama CRS Birmingham, Alabama Sonya Heath, LoR - (slheath@uabmc.edu)
Ann & Robert H Lurie Children's Hospital of Chicago Chicago, Illinois Ellen Chadwick, LoR - (egchadwick@luriechildrens.org)
Barranco CRS Lima, Mey Leon, IoR - (mleon@impactaperu.org)
Baylor College of Medicine / Texas Children's Hospital NICHD CRS Houston, Texas Mary Paul, LoR - (mpaul@bcm.edu)
Brigham and Women's Hospital Therapeutics Boston, Massachusetts Jennifer Manne, LoR - (JManne@BWH.Harvard.edu)
Bronx-Lebanon Hospital Center NICHD CRS New York, New York Murli Purswani, IoR - (mpurswan@bronxcare.org)
Case Western Reserve University CTU Cleveland, Ohio Jeffrey Jacobson, IoR - (jxj573@case.edu)
Centro de Investigaciones Tecnológicas, Biomédicas y Medioambientales CRS (CITBM) - Unidad de Ensayos Clínicos (UNIDEC) CRS Callao, Juan Jose Montenegro, IoR
Centro de Pesquisas Clínicas IC-HCFMUSP CRS São Paulo, Esper Georges Kallas, IoR - (esper.kallas@usp.br)
Centro de Referencia e Treinamento DST/AIDS CRS São Paulo, São Paulo Jose Valdez Madruga, IoR - (valdezmr@uol.com.br)
Cincinnati CRS Cincinnati, Ohio Carl Fichtenbaum, IoR - (FICHTECJ@UCMAIL.UC.EDU)
Columbia Physicians & Surgeons (P&S) CRS New York, New York Jason Zucker, IoR - (jz2700@cumc.columbia.edu)
David Geffen School of Medicine at UCLA NICHD CRS Los Angeles, California Jaime Deville, IoR - (jdeville@mednet.ucla.edu)
Denver Public Health CRS Denver, Colorado Edward Gardner, IoR - (edward.m.gardner@dhha.org)
Duke University Medical Center CRS Durham, North Carolina Cameron Wolfe, IoR - (cameron.wolfe@duke.edu)
Easy Bay AIDS Center CRS City: Oakland Oakland, California Michele Tang, IoR - (michele.tang@sutterhealth.org)
Fundacion Huesped CRS Buenos Aires, Maria Ines Figueroa, IoR - (maria.figueroa@huesped.org.ar)
Harbor University of California Los Angeles Center Torrance, California Eric Daar, IoR - (edaar@lundquist.org)
Harlem Prevention Center New York, New York Sharon Mannheimer, IoR - (sbm20@cumc.columbia.edu)
Henry Ford Hospital CRS Detroit, Michigan Indira Brar, IoR - (ibrar1@hfhs.org)
Hospital Nossa Senhora da Conceicao CRS Porto Alegre, Rio Grande do Sul Breno Santos, IoR - (breno@ghc.com.br)
Houston AIDS Research Team (HART) CRS Houston, Texas Karen Vigil, IoR - (Karen.J.Vigil@uth.tmc.edu)
IMPAACT/ Gamma Project/ UPR Pediatric HIV/AIDS Research CRS San Juan, Irma Febo-Rodriguez, IoR - (irma.febo2@upr.edu)
Infectious Disease Clinical and Translational Research New York, New York Judith Aberg, IoR - (judith.aberg@mssm.edu)
Jacobi Medical Center Bronx NICHD CRS Bronx, New York Andrew Wiznia, IoR - (andrew.wiznia@nychhc.org)
Johns Hopkins University CRS Baltimore, Maryland Matthew Hamill, IoR - (mhamill6@jhu.edu)
Kaiser Permanente Los Angeles Medical Center Los Angeles, California William Towner, IoR - (william.j.towner@kp.org)
Los Angeles LGBT Center CRS Los Angeles, California Robert Bolan, LoR - (bbolan@lalgbtcenter.org)
Massachusetts General Hospital CRS (MGH CRS) Boston, Massachusetts Elizabeth Hohmann, IoR - (EHOHMANN@mgh.harvard.edu)
Mount Sinai West Samuels CRS New York, New York Erna Kojic, IoR - (Erna.Kojic@mountsinai.org)
New Jersey Medical School Clinical Research Center Newark, New Jersey Debra Chew, IoR - (chewde@njms.rutgers.edu)
North Texas Infectious Disease Consultants Dallas, Texas Uriel Sandkovsky, IoR - (uriel.sandkovsky@ntidc.org)
Northwestern University Chicago, Illinois Babafemi Taiwo, IoR - (b-taiwo@northwestern.edu)
Nutricion Mexico CRS Mexico City, Juan Sierra Madero, IoR - (jsmadero@yahoo.com)
Ohio State University CRS Columbus, Ohio Jose Bazan, IoR - (Jose.Bazan@osumc.edu)
Penn Therapeutics CRS Philadelphia, Pennsylvania William Short, IoR - (william.short@pennmedicine.upenn.edu)
Puerto Rico AIDS Clinical Trials Unit CRS San Juan, Jorge Santana, IoR - (jorge.santana3@upr.edu)
Rush University CRS Chicago, Illinois Shivanjali Shankaran, IoR - (Shivanjali_Shankaran@rush.edu)
Rush University Cook County Hospital Chicago NICHD CRS Chicago, Illinois Mariam Aziz, IoR - (mariam_aziz@rush.edu)
SUNY Stony Brook NICHD CRS Stony Brook, New York Sharon Nachman, IoR - (sharon.nachman@stonybrookmedicine.edu)
San Miguel CRS Lima, Jose Antonio Narrea Cango, IoR - (jnarrea@impactaperu.org)
Socios En Salud Sucursal Peru Lima, Augusto Magno Tarazona Fernandez, IoR - (atarazona_ses@pih.org)
Soweto CRS Johannesburg, Lerato Mohapi - (mohapil@phru.co.za)
St. Jude Children's Research Hospital ATN CRS Memphis, Tennessee Katherine Knapp, IoR - (katherine.knapp@stjude.org)
The Ponce de Leon Center CRS Atlanta, Georgia Carlos del Rio, IoR - (cdelrio@emory.edu)
Trinity Health and Wellness Center CRS Dallas, Texas Roger Bedimo, IoR - (Roger.Bedimo@va.gov)
UCLA CARE Center CRS Los Angeles, California Raphael Landovitz, IoR - (rlandovitz@mednet.ucla.edu)
UCSD Antiviral Research Center CRS San Diego, California Susan Little, IoR - (Slittle@health.ucsd.edu)
UT Southwestern Infectious Disease Research Unit Dallas, Texas Ellen Kitchell, IoR - (Ellen.Kitchell@UTSouthwestern.edu)
Univ. of South Florida (USF) College of Medicine A Tampa, Florida Carina Rodriguez, IoR - (crodrig1@usf.edu)
University of California, Davis CRS Sacramento, California Stuart Cohen, IoR - (stcohen@ucdavis.edu)
University of California, San Francisco HIV/AIDS CRS San Francisco, California Annie Luetkemeyer, IoR - (annie.luetkemeyer@ucsf.edu)
University of Colorado Denver NICHD CRS Aurora, Colorado Betsy McFarland, IoR - (Bety.McFarland@cuanschutz.edu)
University of Colorado Hospital CRS Aurora, Colorado Thomas Campbell, IoR - (thomas.campbell@cuanschutz.edu)
University of Florida Gainesville, Florida Nicole Iovine, IoR - (Nicole.Iovine@medicine.ufl.edu)
University of Florida Jacksonville NICHD CRS Jacksonville, Florida Mobeen Rathore, IoR - (mobeen.rathore@jax.ufl.edu)
University of Miami / Jackson Memorial Hospital Miami, Florida Susanne Doblecki-Lewis, IoR - (sdoblecki@med.miami.edu)
University of Miami/Pediatric Perinatal HIV NICHD CRS Miami, Florida Charles Mitchell, IoR - (cmitchel@med.miami.edu)
University of Nebraska Medical Center (Specialty Care Center) Omaha, Nebraska Sara Bares, IoR - (sara.bares@unmc.edu)
University of Pittsburgh CRS Pittsburgh, Pennsylvania Ken Ho, IoR - (hok2@upmc.edu)
University of Rochester Adult HIV Therapeutic Rochester, New York Sonal Munsiff, IoR - (Sonal_Munsiff@URMC.Rochester.edu)
University of Texas, San Antonio San Antonio, Texas Thomas Patterson, IoR - (PATTERSON@uthscsa.edu)
University of Washington Positive Research Seattle, Washington Rachel Bender-Ignacio, IoR - (rbi13@uw.edu)
University of the Witwatersrand Helen Joseph (WITS HJH) Johannesburg, Sharlaa Badal-Faesen, IoR - (sfaesen@witshealth.co.za)
Usc La Nichd Crs Los Angeles, California Mikhaela Cielo, IoR - (mikhaela.cielo@usc.edu)
Vanderbilt Therapeutics CRS Nashville, Tennessee David Haas, IoR - (david.haas@vumc.org)
Via Libre CRS Lima, Jose Alfredo Hidalgo Vidal, IoR - (pepinhidalgo@yahoo.com)
Virginia Commonwealth University Division of Infectious Diseases Richmond, Virginia Akira Shishido, IoR - (Akira.Shishido@vcuhealth.org)
Wake Forest Baptist Medical Center CRS Winston-Salem, North Carolina Aimee Wilkin, IoR - (awilkin@wakehealth.edu)
Washington University Therapeutics (WT) CRS Saint Louis, Missouri Racehl Presti, IoR - (prestir@wustl.edu)
Weill Cornell Chelsea CRS New York, New York Tim Wilkin, IoR - (tiw2001@med.cornell.edu)
Weill Cornell Uptown CRS New York, New York Tim Wilkin, IoR - (tiw2001@med.cornell.edu)
Yale University School of Medicine North Haven, Connecticut Jessica Tuan, IoR - (jessica.tuan@yale.edu)

Study of Posoleucel (ALVR105, Formerly Viralym-M) for Multi-Virus Prevention in Patients Post-Allogeneic Hematopoietic Cell Transplant (Prevent)

Dee Rodriguez - ClinicalTrials@allovir.com

NCT05305040
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Key
Inclusion Criteria:

• ≥1 year of age at the day of screening visit.
• No known or suspected clinically significant disease from AdV, BKV, CMV, EBV, HHV-6, and/or JCV
• Within 15 and 42 days of receiving a first allogeneic HCT and have demonstrated clinical engraftment
• Meet one or more of the following criteria at the time of randomization:
• Related (sibling) donor with at least one mismatch at one of these HLA-gene loci: HLA-A, -B or -DR
• Haploidentical donor
• Matched or Mismatched unrelated donor
• Use of umbilical cord blood as stem cell source
• Ex vivo graft manipulation resulting in T cell depletion
• Received anti-thymocyte globulin or alemtuzumab (Campath-1H) Key
Exclusion Criteria:

• History of AdV, BKV, CMV, EBV, HHV-6, and/or JCV end-organ disease within 6 months prior to randomization
• Evidence of active Grade >2 acute GVHD
• Presence of non-minor uncontrolled or progressive bacterial, viral or fungal infections
• Known history or current (suspected) diagnosis of CRS requiring treatment associated with the administration of peptides, proteins, and/or antibodies
• Ongoing therapy with high-dose systemic corticosteroids (ie, prednisone equivalent dose >0.5 mg/kg/day) within 24 hours prior to dosing
• Relapse of primary malignancy other than minimal residual disease Note: Other protocol defined Inclusion/Exclusion criteria may apply.
Biological: Posoleucel (ALVR105), Biological: Placebo
Adenovirus Infection, BK Virus Infection, Cytomegalovirus Infections, Epstein-Barr Virus Infections, Human Herpes Virus-6 Infection, JC Virus Infection
Allogeneic Hematopoietic Cell Transplant, ALVR105, Posoleucel, Viralym-M
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A.Z. St. Jan Brugge,
Acibadem Adana Hospital Seyhan,
Addenbrooke's Hospital Cambridge,
Alberta Children's Hospital Calgary, Alberta
Anadolu Medical Center Hospital Gebze,
Ankara Abdurrahman Yurtaslan Hospital Ankara,
Ankara University Medical Faculty Ankara,
Azienda Ospedaliera Universitaria Integrata Verona-Ospedale Borgo Trento Verona,
Azienda Ospedaliero-Universitaria Careggi Florence,
Barns Jewish Hospital Saint Louis, Missouri
Baskent Adana Hospital Adana,
Bristol Haematology and Oncology Centre Bristol,
CHU de Nantes Nantes,
Cellular Therapy Program - CHU Sainte-Justine (McGill) Québec,
Centre Hospitalier Lyon Sud Pierre-Bénite,
Centre Hospitalier Regional Universitaire de Lille Lille,
Cheonam National University Hwasun Hospital Hwasun,
Children's Medical Center Dallas Dallas, Texas
Children's Mercy Hospital - Kansas City Kansas City, Missouri
Children's National Medical Center Washington D.C., District of Columbia
Childrens National Health System Washington, District of Columbia
City of Hope Duarte, California
Columbia University New York, New York
Dana Farber Cancer Institute Boston, Massachusetts
Ege University Medical Faculty Izmir,
Fondazione I.R.C.C.S. Policlinico San Matteo Pavia,
Fondazione Policlinico Universitario A. Gemelli IRCCS - Universita Cattolica del Sacro Cuore Rome,
Fred Hutchinson Cancer Research Center Seattle, Washington
Froedtert Hospital and the Medical College of Wisconsin Milwaukee, Wisconsin
Gazi University Medical Faculty Hospital Ankara,
Great Ormond Street Hospital For Children London,
Hackensack University Medical Center Hackensack, New Jersey
Honor Health Scottsdale, Arizona
Hopital Maisonneve Rosemont Montreal,
Hopital Saint Antoine Paris,
Hopital Universitaire Robert Debre Paris,
Hospital General Universitario Gregorio Marañon Madrid,
Hospital Saint-Louis Paris,
Hospital Universitari i Politecnic La Fe de Valencia Valencia,
IRCCS Ospedale San Raffaele Milan,
Indiana University Hospital Indianapolis, Indiana
Inonu University Turgut Özal Medical Centre Malatya,
Institut Catala d'Oncologia Barcelona,
Institut Claudius Regaud Cancer Comprehensive Center - IUCT Oncopole Toulouse,
Institut Jules Bordet and the Childrens Hospital Anderlecht,
Istituto Clinico Humanitas Rozzano (MI),
King's College Hospital London,
Leukemia/BMT Program of British Columbia Vancouver,
Levine Cancer Center Charlotte, North Carolina
Loyola University Maywood, Illinois
MOFFITT Tampa, Florida
Medical Park Hospital Istanbul,
Nationwide Children's Hospital Columbus, Ohio
Northside Hospital Atlanta, Georgia
Olivia Newton John Hospital Heidelberg,
Oregon Health & Science University Portland, Oregon
Ospedale Pediatrico Bambino Gesu Rome,
Pusan National University Hospital Busan,
Queen Elizabeth University Hospital Glasgow,
Queensland Children's Hospital South Brisbane, Queensland
Roswell Park Comprehensive Cancer Center Buffalo, New York
Royal Adelaide Hospital Adelaide, South Australia
Royal Brisbane and Women's Hospital Herston, Queensland
Royal Melbourne Hospital Parkville, Victoria
Samsung Medical Center Seoul, Gangnam-gu
Seoul National University Hospital Seoul, Seoul Teugbyeolsi
Seoul St. Mary's Hospital, The Catholic University of Korea Seoul,
Severance Hospital, Yonsei University Health System Seoul,
St Vincents Hospital Sydney Limited Darlinghurst,
Stanford University Palo Alto, California
Stony Brook University Hospital Cancer Center Stony Brook, New York
The Hospital for Sick Children Blood & Marrow Transplant / Cellular Therapy Program Toronto,
UCLA Santa Monica, California
UHN Blood and Marrow Transplant (BMT) Program (Princess Margaret) Toronto,
Unidad De Hemofilia, Hospital Regional Universitario De Malaga Málaga,
University Hospital Gasthuisberg and Leuven Leuven,
University Hospitals Bristol Bristol,
University Utah Childrens Hospital Salt Lake City, Utah
University of Alabama at Birmingham Birmingham, Alabama
University of California, San Francisco Medical Center San Francisco, California
University of Chicago Chicago, Illinois
University of Colorado Hospital Aurora, Colorado
University of Florida - Division of Hematology & Oncology Gainesville, Florida
University of Kansas Cancer Center Kansas City, Kansas
University of Maryland Medical Center Baltimore, Maryland
University of Minnesota Minneapolis, Minnesota
University of Pennsylvania Philadelphia, Pennsylvania
University of Sacred Heart Policlinico A. Gemelli Rome,
University of Virginia Charlottesville, Virginia
Vanderbilt University Medical Center Nashville, Tennessee
Virginia Commonwealth University Richmond, Virginia
Washington University School of Medicine St Louis, Missouri
Weil Medical College - NY Presbyterian Hospital New York, New York
Westmead Hospital Westmead,
Yale University School of Medicine North Haven, Connecticut

A Study of Amivantamab and Capmatinib Combination Therapy in Unresectable Metastatic Non-small Cell Lung Cancer (METalmark)

Study Contact - Participate-In-This-Study@its.jnj.com

NCT05488314
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Inclusion Criteria:

• Previously diagnosed with histologically or cytologically confirmed unresectable Stage IV (metastatic) non-small cell lung cancer (NSCLC) (any histology)
• May have: definitively, locally treated brain metastases that are clinically stable and asymptomatic for greater than (>) 2 weeks and who are off or receiving low-dose corticosteroid treatment (less than or equal to [<=]10 milligrams (mg) prednisone or equivalent) for at least 2 weeks prior to start of study treatment
• May have a prior malignancy (other than the disease under study) the natural history or treatment of which is unlikely to interfere with any study endpoints of safety or the efficacy of the study treatment(s)
• Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• A female participant of childbearing potential must have a negative serum pregnancy test at screening and within 72 hours of the first dose of study treatment and must agree to further serum or urine pregnancy tests during the study
Exclusion Criteria:

• Medical history of (non-infectious) interstitial lung disease (ILD)/pneumonitis, or has current ILD/pneumonitis, or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening
• Participant has impairment of the gastrointestinal function that could affect absorption of capmatinib or is unable or unwilling to swallow tablets
• Participant has symptomatic central nervous system (CNS) metastases which are neurologically unstable or have required increasing doses of steroids >10 mg prednisone or equivalent within the 2 weeks prior to study entry to manage CNS symptoms
• Participant has uncontrolled tumor-related pain: Symptomatic lesions amenable to palliative radiotherapy (example, bone metastases, or metastases causing nerve impingement) should be treated more than 7 days prior to the administration of the first study treatment
Drug: Capmatinib, Drug: Amivantamab
Carcinoma, Non-Small-Cell Lung
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ASST Grande Ospedale Metropolitano Niguarda Milan,
Ankara Bilkent City Hospital Ankara,
Asan Medical Center SongpaGu, Seoul Teugbyeolsi
Auxilio Mutuo Cancer Center San Juan,
Beijing Cancer Hospital Beijing,
CHU de la Timone Marseille,
CIONC - Centro Integrado de Oncologia de Curitiba Curitiba, Paraná
Centre Leon Berard Lyon,
Charite Universitaetsmedizin Berlin Berlin,
Chongqing University Cancer Hospital Chongqing, Chongqing Municipality
Chonnam National University Hwasun Hospital Jeollanam-do,
Chungbuk National University Hospital Cheongju-si, North Chungcheong
Dana-Farber Cancer Institute Boston, Massachusetts
Fondazione G. Pascale - Istituto Nazionale Tumori IRCCS Napoli,
Fondazione IRCCS Istituto Nazionale dei Tumori Milan,
Fudan University Shanghai Cancer Center Shanghai,
Fundação Antônio Prudente - A.C. Camargo Cancer Center Sao Paulo,
Gachon University Gil Hospital Incheon,
Gazi University Hospital Ankara,
Goztepe Prof. Dr. Suleyman Yalcin Sehir Hastanesi Istanbul,
H. Lee Moffitt Cancer & Research Institute Tampa, Florida
Harbin Medical University Cancer Hospital Harbin, Heilongjiang
Helios Klinikum Emil von Behring GmbH Berlin,
Henan Cancer Hospital Zhengzhou, Henan
Hosp. Clinic I Provincial de Barcelona Barcelona,
Hosp. Clinico Univ. de Valencia Valencia,
Hosp. Del Mar Barcelona,
Hosp. Gral. Univ. de Alicante Alicante,
Hosp. Univ. 12 de Octubre Madrid,
Hosp. Univ. A Coruña A Coruña,
Hosp. Univ. Fund. Jimenez Diaz Madrid,
Hosp. Univ. La Paz Madrid,
Hosp. Univ. Quiron Dexeus Barcelona,
Hosp. Univ. Vall D Hebron Barcelona,
Hosp. Virgen Macarena Sevilla,
Huizhou Municipal Central Hospital Huizhou,
INSTYTUT GENETYKI I IMMUNOLOGII GENIM Sp. z o.o. Lublin,
Imperial College London and Imperial College Healthcare NHS Trust London,
Institut Curie Paris,
Institut de Cancerologie de l'Ouest Saint-Herblain,
Institute Coeur Poumon Lille,
Instituto D'Or de Pesquisa e Ensino (IDOR) São Paulo,
Istanbul University Cerrahpasa Medical Faculty Istanbul, Bakirkoy
Istituto Nazionale Tumori Regina Elena Rome,
Istituto Oncologico Veneto - IRCCS Padova,
Klinikum Chemnitz gGmbH Chemnitz,
Liv Hospital Ankara Ankara,
Medical College of Wisconsin Milwaukee, Wisconsin
Memorial Ankara Hastanesi Ankara,
Montefiore Einstein Center for Cancer Care The Bronx, New York
Munchen Klinik GmbH Klinik Bogenhausen München,
Narodowy Instytut Onkologii im. Marii Sklodowskiej-Curie - Panstwowy Instytut Badawczy Warszawa,
National Cancer Center Goyang-si,
National Hospital Organization Nagoya Medical Center Nagoya, Aichi-ken
Nouvel Hopital Civil - CHU Strasbourg Strasbourg cedex,
Núcleo de Oncologia da Bahia Salvador,
Oncoclínicas Rio de Janeiro S.A. Rio de Janeiro,
Ospedale S. Maria Delle Croci Ravenna,
PERSONAL - Oncologia de Precisão e Personalizada Belo Horizonte,
Providence Portland Medical Center Portland, Oregon
Royal Marsden Hospital London,
Second Affiliated Hospital, School of Medicine, Zhejiang University Hangzhou,
Seoul National University Bundang Hospital Seongnam-si, Gyeonggi-do
Seoul National University Hospital Seoul, Seoul Teugbyeolsi
Severance Hospital, Yonsei University Health System Seoul,
Shanghai Pulmonary Hospital Shanghai,
Shengjing Hospital of China Medical University Shenyang,
Shizuoka Cancer Center Nagaizumi-chō,
Sichuan Cancer Hospital Chengdu,
Sir Bobby Robson Cancer Trials Research Centre Newcastle upon Tyne,
Sir Run Run Shaw Hospital, Zhejiang University School of Medicine Hangzhou,
Sociedade Beneficente de Senhoras - Hospital Sírio Libanês Buenos Aires,
The Cancer Institute Hospital of JFCR Koto-ku, Tokyo
The First Affiliated Hospital of Xi'An Jiaotong University Xi’an, Shanxi
The First Affiliated Hospital, Sun Yat-sen University Guangzhou, Guangdong
The First Affiliated Hospital, Zhejiang University College of Medicine Hangzhou,
The Oncology Institute of Hope and Innovation Fort Lauderdale, Florida
The Ottawa Hospital Research Institute Ottawa, Ontario
UCLA Santa Monica, California
UPCO Unidade de Pesquisa Clinica em Oncologia Pelotas,
Universitaetsklinikum Carl Gustav Carus TU Dresden Dresden,
Universitaetsklinikum Essen Essen,
Universitaetsklinikum Koeln Cologne,
Universitaetsklinikum Muenster Münster,
University College London Hospitals NHS Foundation Trust London, Greater London
University Health Network (UHN) Princess Margaret Cancer Centre Toronto, Ontario
University of Alabama at Birmingham, Comprehensive Cancer Center Birmingham, Alabama
University of California, Irvine Orange, California
University of Chicago Chicago, Illinois
University of North Carolina Chapel Hill, North Carolina
Uniwersyteckie Centrum Kliniczne Gdansk,
União Brasileira de Educação e Assistência-Hospital São Lucas da PUCRS Porto Alegre,
VCU Medical Center Richmond, Virginia
Virginia Cancer Specialists Fairfax, Virginia
West China Hospital, Sichuan University Chengdu, Sichuan
Yantai Yuhuangding Hospital Yantai, Shandong

LGMD R1 Natural History Study (GRASP-01-003)

Ruby Langeslay - ruby.langeslay@vcuhealth.org

NCT05618080
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Inclusion Criteria:

• Age between 12-50 at enrollment
• Clinically affected (defined as weakness on bedside evaluation in a pattern consistent with LGMDR1)
• Genetic confirmation of LGMDR1 (presence of homozygous or compound heterozygous pathogenic mutations in CAPN3).
• Must be able to provide written informed consent and be willing and able to comply with all study requirements. Note: Adult participants must be able to provide consent themselves. Legally authorized representatives are not permitted to consent on behalf of adult participants.
Exclusion Criteria:

• Have contraindications to MRI or MRS (e.g., non-MR compatible implanted medical devices or severe claustrophobia)
• Non-ambulatory as defined by those who are not able to walk 10 meters without assistive devices (ankle foot orthotics excluded)
• Positive pregnancy test at any timepoint during the trial
• Have dominantly inherited CAPN3 mutations (LGMDD4)
• Any other illness that would interfere with the ability to undergo safe testing or would interfere with interpretation of the results in the opinion of the site investigator.
Calpain-3 Deficiency Limb Girdle Muscular Dystrophy Type 2A, Limb Girdle Muscular Dystrophy, Limb Girdle Muscular Dystrophy Type R1, LGMD2A
LGMD, Limb Girdle Muscular Dystrophy, LGMD R1, LGMD2A, CAPN3
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Leiden University Medical Center Leiden, Marjolein van Heur - (m.j.van_heur-neuman@lumc.nl) Anne-Marie Peters - (a.m.g.h.Peters@lumc.nl)
Nationwide Children's Hospital Columbus, Ohio Audrey Knight - (audrey.knight@nationwidechildrens.org) Lauren Humphrey - (lauren.humphrey@nationwidechildrens.org)
Newcastle University Newcastle upon Tyne, Tyne and Wear Sonia Segovia - (sonia.segovia@newcastle.ac.uk)
The Community Health Clinic, Inc. Shipshewana, Indiana Grace Lewis - (glewis@indianachc.org)
University of California, Irvine Orange, California Siddhant Pratap - (spratap1@hs.uci.edu) Isela Hernandez - (iselah@hs.uci.edu)
University of Colorado Anschutz Medical Campus Aurora, Colorado Alyssa Avilez - (alyssa.avilez@cuanschutz.edu) Talia Strahler - (talia.strahler@cuanschutz.edu)
University of Florida Gainesville, Florida Yara Mohammed, MD, MPH - (yaramohamed@peds.ufl.edu)
University of Iowa Hospitals and Clinics Iowa City, Iowa Chandra Miller - (chandra-miller@uiowa.edu) Carrie Stephan - (carrie-stephan@uiowa.edu)
University of Kansas Medical Center Kansas City, Kansas Rebecca Clay - (rclay@kumc.edu)
University of Minnesota, Department of Neurology Minneapolis, Minnesota Allison Johnston - (joh21779@umn.edu)
Virginia Commonwealth University Richmond, Virginia Levi Headrick - (levi.headrick@vcuhealth.org) Anarosa, Rezeq - (anarosa.rezeq@vcuhealth.org)
Washington University School of Medicine St Louis, Missouri Olivia Money - (moneyo@wustl.edu)

Periaqueductal Gray-vagus Nerve Interface Malfunction Explain the Natural History With Its Numerous Co-morbidities?

Gisela Chelimsky, M.D. - gisela.chelimsky@vcuhealth.org

NCT05618054
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Inclusion Criteria:
* Females 12-21 years old * Able to communicate and provide consent/assent * English speaking * Diagnosed with POTS (POTS will be defined standardly as a symptomatic ≥ 40 bpm rise in heart rate without a drop in blood pressure and with symptoms of orthostatic intolerance clinically) * Age-matched healthy control subjects: no POTS or other neurological disorders
Exclusion Criteria:
* Inflammatory arthritis, connective tissue or auto-immune disorder * Any chronic neurological disorder besides POTS * Evidence of unstable medical disorder, such as kidney (rising creatinine, or end-stage renal failure) or liver impairment (rising AST or ALT, or end-stage with coagulopathy), poorly controlled significant cardiovascular (CHF), respiratory, endocrine (diabetes - A1c \> 9 - or untreated thyroid dysfunction) or uncontrolled psychiatric illness (such as untreated depression, psychosis, etc.) * Neuropathy, central nervous system disorder (e.g., Cerebral palsy, developmental delay, seizure disorder, MS, stroke, etc.) * Treatment with a drug or medical device within the previous 30 days that has not received regulatory approval * Use of hormones (except insulin, thyroid replacement or oral contraceptives, which will be carefully documented) * Current substance or alcohol abuse * Any major surgical intervention with general anesthesia in the last 60 days and minor procedure, such as tooth extraction, endoscopy, etc., with local or conscious sedation within 7 days * Any on-going or pending medical, health or disability related litigation, or current pursuit of disability * Any condition that in the judgment of the investigator would interfere with the patient's ability to provide informed consent, comply with study instructions, place the patient at increased risk, or which would clearly confound the interpretation of the study results (specific reason will be documented) * Chronic use of narcotics for pain * Claustrophobia or any metal hardware that may interfere with MRI * Investigators and study staff
BEHAVIORAL: Looming task
Postural Tachycardia Syndrome
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Virginia Commonwealth University Richmond, Virginia

Upifitamab Rilsodotin Maintenance in Platinum-Sensitive Recurrent Ovarian Cancer (UP-NEXT) (UP-NEXT)

Rita Lemming - medicalinformation@mersana.com

NCT05329545
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Inclusion Criteria:

• Participant must have a histological diagnosis of high grade serous ovarian cancer, which includes fallopian tube and primary peritoneal cancer, that is metastatic or recurrent.
• Participant must have platinum-sensitive recurrent disease, defined as having achieved either a partial or complete response to 4 or more cycles in their penultimate platinum- containing regimen and their disease progressing more than 6 months after completion of the last dose of platinum containing therapy in the penultimate regimen.
• Participant must have had 4 to 8 cycles of platinum-based chemotherapy in 2nd to 4th line setting in their most recent treatment regimen as defined below:
• Platinum-based chemotherapy regimens allowed immediately preceding enrollment to the study: carboplatin or cisplatin ±: paclitaxel, docetaxel, pegylated liposomal doxorubicin or gemcitabine.
• Participant must receive first study treatment infusion between 4 and 12 weeks after completing final dose of platinum in the most recent platinum-based regimen.
• Participant must have had as their best response to last line of treatment one of the following: No Evidence of Disease (NED); Complete Response (CR); Partial Response (PR); OR Stable Disease (SD)
• Participants with NED, CR, or PR as their best response to most recent line of treatment and who have not received treatment with a prior PARP inhibitor must have definitive BRCA1 and BRCA2 testing results that demonstrate no evidence of a deleterious BRCA1 or BRCA2 mutation. Somatic BRCA mutation testing is required for participants who are classified as not having a deleterious mutation by germline testing alone.
• Participant must provide either a tumor tissue block or fresh cut slides for measurement of NaPi2b expression by a central laboratory. If sufficient archival tumor tissue is not available, then a tumor tissue block or slides must be obtained from a fresh biopsy and provided to the central laboratory. Confirmation of a NaPi2b-H/positive tumor by the central laboratory is required prior to randomization.
Exclusion Criteria:

• Participant has received prior treatment with mirvetuximab soravtansine or another ADC containing an auristatin or maytansinoid payload.
• Participant has received bevacizumab in combination with last platinum-based regiment or plans to receive maintenance therapy outside the study intervention.
• Participant has clinical signs or symptoms of gastrointestinal obstruction and/or requirement for parenteral hydration or nutrition.
• Participant has ascites or pleural effusion managed with therapeutic paracentesis or thoracentesis within 28 days prior to signing the principal study consent form.
• Participant has history of cirrhosis, hepatic fibrosis, esophageal or gastric varices, or other clinically significant liver disease. Testing beyond laboratory studies otherwise defined in the eligibility criteria, to diagnose potentially clinically significant liver disease based on risk factors such as hepatic steatosis or history of excessive alcohol intake, will be based on clinical judgement of the investigator.
• Participant has history of or suspected pneumonitis or interstitial lung disease.
• Participant has untreated CNS metastases (including new and progressive brain metastases), history of leptomeningeal metastasis, or carcinomatous meningitis.
Drug: Upifitimab rilsodotin, Other: Placebo
High Grade Serous Ovarian Cancer, Fallopian Tube Cancer, Primary Peritoneal Cancer
Ovarian Cancer, Serous, Maintenance, Antibody Drug Conjugate, Recurrent, Platinum-Sensitive, ADC, Fallopian Tube Cancer, Primary Peritoneal Cancer
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Study Locations

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Allegheny Health Network Cancer Institute, West Penn Hospital Pittsburgh, Pennsylvania Janke Mains-Mason
Asplundh Cancer Pavilion Willow Grove, Pennsylvania Anam Maqsood
Avera McKennan d/b/a Avera Research Institute Sioux Falls, South Dakota Teri Kayl
Billings Clinic Billings, Montana Kim Bosket
CHUM - University of Montreal Hospital Centre Montréal, Quebec Genevieve St-Onge
Carilion Clinic Gynecological Oncology Roanoke, Virginia Danielle Mitchell
Center of Hope Reno, Nevada Shannon Pierpoint
Cleveland Clinic - Cleveland Cleveland, Ohio Leslie Jones
Community Health Network, Community Cancer Center North Indianapolis, Indiana Alexandra Gray
Cox Medical Centers, GYN ONC Springfield, Missouri Aimee Caldwell
Dartmouth Hitchcock Medical Center Lebanon, New Hampshire Rebecca Dabrowski
Epworth Richmond Richmond, Victoria
Erlanger Womens Oncology Chattanooga, Tennessee Kimberly Donelson
Froedtert Hospital and the Medical College of Wisconsin Milwaukee, Wisconsin Jacklyn Schmid
Greater Baltimore Medical Center Baltimore, Maryland Melissa Loomis
Gyne Oncology Clinic Hinsdale, Illinois Jan Miller
Hackensack University Medical Center, John Theurer Cancer Center Hackensack, New Jersey Aretha DiSalvo
Hollings Cancer Center (HCC) Charleston, South Carolina Vistea Crawford
Holy Name Medical Center Teaneck, New Jersey Precious Akinsanya
HonorHealth Research Institute - HonorHealth VGPCC Biltmore Phoenix, Arizona Abigale Hamlin
Icon Cancer Centre - Chermside Chermside, Queensland Jesse Peet
Icon Cancer Centre Southport Southport, Queensland Troy Wood
Icon Cancer Centre Wesley Auchenflower, Deanne Russell
Karmanos Cancer Institute - Detroit Detroit, Michigan Leah Dunham
Kettering Health Cancer Center Kettering, Ohio Molly Moore
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York, New York Monica Gill
Legacy Good Samaritan Medical Center - Legacy Medical Group - Gynecologic Oncology Portland, Oregon Michael Jung
Levine Cancer Institute Charlotte, North Carolina Leah Wilson
Maine Medical Partners, Division of Gynecologic Oncology Scarborough, Maine Robin Donovan
Methodist Hospital Saint Louis Park, Minnesota Mary Beth Wilwerding
MidAmerica Division, Inc., c/o Research Medical Center Kansas City, Missouri Katie Burnside
Minnesota Oncology Hematology, P.A. Maple Grove, Minnesota Brianna Lenox
Mount Sinai Comprehensive Cancer Center Miami Beach, Florida Ana Lacombe
Northeast Georgia Medical Center Gainesville, Georgia Melissa Shaw
Northwest Cancer Specialists PC Vancouver, Washington Susan Papenfuse
OSU Gynecologic Oncology at Mill Run Hilliard, Ohio Kelly Dodd
Orlando Health, Inc. Orlando, Florida Michael Todd Roberts
Perelman Center for Advanced Medicine Philadelphia, Pennsylvania Isabel Forbes
Rocky Mountain Cancer Centers - Aurora Aurora, Colorado Brandon Keith
Sarasota Memorial Hospital Sarasota, Florida Angela Price
Southwest Women's Oncology Albuquerque, New Mexico Robert Kushner
Stephenson Cancer Center Oklahoma City, Oklahoma Erin Hemken
Tampa General Hospital Tampa, Florida Martin Marlene
Texas Oncology - DFWW Bedford, Texas Hannah Hirad
Texas Oncology - Dallas Presbyterian Hospital The Woodlands, Texas Libby Brandenburg
Texas Oncology - Fort Worth Cancer Center Fort Worth, Texas Cynthia Schoenfeldt
Texas Oncology - Tyler Tyler, Texas K. Shelly Maxfield
Texas Oncology P.A. - Austin Austin, Texas Alfonzo Paredes
Texas Oncology P.A. - McAllen McAllen, Texas Aide Borrego
The Blavatnik Family at Chelsea Medical Center at Mount Sinai New York, New York Siddhi Nilesh Savla
The University of Arizona Cancer Center Tucson, Arizona Belen Mejia
University Hospitals Cleveland Medical Center, Seidman Cancer Center Cleveland, Ohio Nancy Fusco
University of California Los Angeles, Gynecologic Oncology Clinic Los Angeles, California Dominique Fahmy
University of California, Irvine Medical Center Orange, California Nidhisha Patel
University of Chicago Medical Center Chicago, Illinois Alexandra Larkin
University of Cincinnati Medical Center Cincinnati, Ohio Eleanor Grethel
University of New Mexico Cancer Center Albuquerque, New Mexico Sheri Westgate
University of Wisconsin Clinical Science Center Madison, Wisconsin Nichole Blazel
VCU Massey Cancer Center Richmond, Virginia Sonya Washington
Vidant Cancer Center - at Vidant Medical Center Greenville, North Carolina Tamika Little
WK Physicians Shreveport, Louisiana Carrie Kay
Washington University School of Medicine, Center for Advanced Medicine Saint Louis, Missouri Krystal Martin
Willamette Valley Cancer Institute and Research Center Eugene, Oregon Jeanne Schaffer
Women and Infants Hospital Providence, Rhode Island Ann John
Women's Cancer Center of Nevada Las Vegas, Nevada Jacky Amador

Testing the Addition of Ipatasertib to Usual Chemotherapy and Radiation for Head and Neck Cancer

ctrrecruit@vcu.edu

NCT05172245
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Inclusion Criteria:
* Patients must have pathologically confirmed HNSCC (including tumors of the oropharynx, hypopharynx, larynx, oral cavity, nasal cavity, maxillary and other paranasal sinuses, and unknown primary of the head and neck), with measurable disease as per RECIST 1.1 * Oropharyngeal and unknown primary squamous cell cancers must test for human papilloma virus (HPV), for example by p16 immunohistochemistry (IHC), in situ hybridization (ISH), or polymerase chain reaction (PCR). HPV testing is not required for other HNSCC primary tumor sites * Patients with p16-positive tumors are eligible if clinical stage III (cT4 or cN3, M0) according to the American Joint Committee on Cancer (AJCC)/TNM Staging System, 8th edition (Ed.) * Patients with p16-negative (or not tested) tumors are eligible if clinical stage III-IVB (locally advanced but non-metastatic) according to the AJCC/TNM Staging System, 8th Ed. * Must be candidate for concurrent, definitive cisplatin and radiation therapy as judged by the treating physician * Able to swallow tablets at the time of enrollment * Age \>= 18 years. Because no dosing or adverse event data are currently available on the use of ipatasertib in combination with chemoradiation in patients \< 18 years of age, children are excluded from this study * Eastern Cooperative Oncology Group (ECOG) performance status 0-1 * Life expectancy of greater than 3 months * Absolute neutrophil count \>= 3000/mcL * Hemoglobin \>= 10 g/dL * Platelets \>= 150,000/mcL * Serum albumin \>= 3 g/dL * Total bilirubin =\< 1.5 x institutional upper limit of normal (ULN) * Aspartate aminotransferase (AST) (serum glutamic oxaloacetic transaminase \[SGOT\])/alanine aminotransferase (ALT) (serum glutamate pyruvate transaminase \[SGPT\]) =\< 2.5 x institutional ULN / 2 x institutional ULN * Alkaline phosphatase (ALP) =\< 2.0 x institutional ULN * Partial thromboplastin time (PTT) (or activated \[a\]PTT) and international normalized ratio (INR) =\< 1.5 institutional ULN (except for patients receiving anticoagulation therapy) * Creatinine clearance (CLcr) \> 60 mL/min * For this calculation, use the Cockroft-Gault formula * Fasting glucose =\< 150 mg/dL (8.3 mmol/L) and (when indicated) glycosylated hemoglobin (HbA1c ) =\< 7.5% (58 mmol/mol) * Human immunodeficiency virus (HIV)-infected patients are eligible if on effective anti-retroviral therapy with undetectable viral load within 6 months * Patients with past hepatitis B virus (HBV) infection or resolved HBV infection (defined as having a negative hepatitis B virus surface antigen \[HBsAg\] test and a positive hepatitis B core antibody \[HBcAb\] test, accompanied by a negative HBV deoxyribonucleic acid \[DNA\] test) are eligible. Patients with chronic HBV infection are eligible if the HBV viral load is undetectable on suppressive therapy, if indicated. Patients undergoing current treatment with anti-viral therapy for HBV are ineligible * Patients with a history of hepatitis C virus (HCV) infection are eligible only if polymerase chain reaction (PCR) is negative for HCV ribonucleic acid (RNA). Patients with HCV infection who are currently on treatment are eligible if they have an undetectable HCV viral load * Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial * The effects of ipatasertib on the developing human fetus are unknown. For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive methods with a failure rate of \< 1% per year during the treatment period and for at least 28 days after the last dose of ipatasertib and agreement to refrain from donating eggs during this same period. For men: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures, and agreement to refrain from donating sperm during the treatment period and for 28 days after the last dose of ipatasertib * Ability to understand and the willingness to sign a written informed consent document * For the expansion cohort only, patients must agree to undergo mandatory on-treatment biopsies, and have tumors amenable to on-treatment biopsies. This is not applicable to the dose escalation cohort where no on-treatment biopsies are obtained
Exclusion Criteria:
* Primary tumor of nasopharynx, salivary, thyroid or parathyroid glands, or skin * Distant metastases from the current HNSCC * Prior treatment (e.g., chemotherapy, radiation, or definitive surgery) for the current locally advanced HNSCC is not permitted. Biopsies, including those performed under anesthesia, are not considered surgery. Patients who underwent prior definitive surgery alone for an early stage (T1-2N0) HNSCC which has now recurred with stage III-IVB disease at least 3 months after the initial surgery are eligible * For patients with a prior history of another malignancy, no prior chemotherapy or radiation may have been administered within 6 weeks prior to study entry. Among patients who received prior radiation to the head and neck or adjacent anatomical site for another malignancy, there may be no overlap with current area to be irradiated * Current use of any other investigational agents * History of allergic reactions attributed to compounds of similar chemical or biologic composition to ipatasertib or other agents used in study * Treatment with strong inhibitors or inducers of CYP3A4 or P-glycoprotein within 2 weeks or 5 drug-elimination half-lives, whichever is longer, prior to initiation of study drug. Because the lists of these agents are constantly changing, it is important to regularly consult a frequently-updated medical reference. As part of the enrollment/informed consent procedures, the patient will be counseled on the risk of interactions with other agents, and what to do if new medications need to be prescribed or if the patient is considering a new over-the-counter medicine or herbal product * Patients with uncontrolled intercurrent illness, including active infection * Pregnant women are excluded from this study because ipatasertib is an oral AKT inhibitor with the potential for teratogenic or abortifacient effects. Because there is an unknown but potential risk for adverse events in nursing infants secondary to treatment of the mother with ipatasertib, breastfeeding should be discontinued if the mother is treated with ipatasertib. These potential risks may also apply to other agents used in this study * Patients with type I or type II diabetes mellitus requiring insulin at study entry. Patients with non-insulin dependent type II diabetes mellitus are eligible, as are patients who are on a stable dose of oral diabetes medication \>= 4 weeks prior to initiation of study treatment. Patients with a history of diabetes mellitus, an abnormal fasting glucose level, or other signs or symptoms indicating diabetes mellitus, must meet the laboratory eligibility criteria for fasting blood glucose and hemoglobin A1c * History of or active inflammatory bowel disease (e.g., Crohn's disease and ulcerative colitis) or active bowel inflammation (e.g., diverticulitis) * History of malabsorption syndrome or other condition that would interfere with enteral absorption or results in the inability or unwillingness to swallow pills * Lung disease: pneumonitis, interstitial lung disease, idiopathic pulmonary fibrosis, cystic fibrosis, aspergillosis, active tuberculosis, or history of opportunistic infections (pneumocystis pneumonia or cytomegalovirus pneumonia) * Known clinically significant history of liver disease consistent with Child Pugh Class B or C, including active viral or other hepatitis (e.g., positive for hepatitis B surface antigen \[HBsAg\] or hepatitis C virus \[HCV\] antibody at screening), or cirrhosis * Grade \>= 2 uncontrolled or untreated hypercholesterolemia (cholesterol \> 300 mg/dL or \> 7.75 mmol/L) or hypertriglyceridemia (triglycerides \> 300 mg/dL or \> 3.42 mmol/L)
PROCEDURE: Biopsy Procedure, PROCEDURE: Biospecimen Collection, DRUG: Cisplatin, PROCEDURE: Computed Tomography, DRUG: Ipatasertib, PROCEDURE: Magnetic Resonance Imaging, PROCEDURE: Positron Emission Tomography, RADIATION: Radiation Therapy
Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8, Head and Neck Carcinoma of Unknown Primary, Locally Advanced Head and Neck Squamous Cell Carcinoma, Locally Advanced Hypopharyngeal Squamous Cell Carcinoma, Locally Advanced Laryngeal Squamous Cell Carcinoma, Locally Advanced Nasal Cavity Squamous Cell Carcinoma, Locally Advanced Oral Cavity Squamous Cell Carcinoma, Locally Advanced Oropharyngeal Squamous Cell Carcinoma, Locally Advanced Paranasal Sinus Squamous Cell Carcinoma, Locally Advanced Sinonasal Squamous Cell Carcinoma, Maxillary Sinus Squamous Cell Carcinoma, Stage III Hypopharyngeal Carcinoma AJCC v8, Stage III Laryngeal Cancer AJCC v8, Stage III Lip and Oral Cavity Cancer AJCC v8, Stage III Oropharyngeal (p16-Negative) Carcinoma AJCC v8, Stage III Sinonasal Cancer AJCC v8, Stage IVA Hypopharyngeal Carcinoma AJCC v8, Stage IVA Laryngeal Cancer AJCC v8, Stage IVA Lip and Oral Cavity Cancer AJCC v8, Stage IVA Oropharyngeal (p16-Negative) Carcinoma AJCC v8, Stage IVA Sinonasal Cancer AJCC v8, Stage IVB Hypopharyngeal Carcinoma AJCC v8, Stage IVB Laryngeal Cancer AJCC v8, Stage IVB Lip and Oral Cavity Cancer AJCC v8, Stage IVB Oropharyngeal (p16-Negative) Carcinoma AJCC v8, Stage IVB Sinonasal Cancer AJCC v8
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Study Locations

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Atrium Health Cabarrus/LCI-Concord Concord, North Carolina
Carolinas Medical Center/Levine Cancer Institute Charlotte, North Carolina
Moffitt Cancer Center Tampa, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Montefiore Medical Center - Moses Campus The Bronx, New York Site Public Contact - (eskwak@montefiore.org)
Montefiore Medical Center-Einstein Campus The Bronx, New York Site Public Contact - (eskwak@montefiore.org)
Northwestern University Chicago, Illinois Site Public Contact - (cancer@northwestern.edu)
Rutgers Cancer Institute of New Jersey New Brunswick, New Jersey
Rutgers New Jersey Medical School Newark, New Jersey
University Health Network-Princess Margaret Hospital Toronto, Ontario
University of Cincinnati Cancer Center-UC Medical Center Cincinnati, Ohio Site Public Contact - (cancer@uchealth.com)
University of Cincinnati Cancer Center-West Chester West Chester, Ohio Site Public Contact - (cancer@uchealth.com)
University of Kansas Cancer Center Kansas City, Kansas Site Public Contact - (KUCC_Navigation@kumc.edu)
University of Kansas Clinical Research Center Fairway, Kansas Site Public Contact - (KUCC_Navigation@kumc.edu)
University of Kansas Hospital-Westwood Cancer Center Westwood, Kansas Site Public Contact - (KUCC_Navigation@kumc.edu)
University of Kentucky/Markey Cancer Center Lexington, Kentucky
University of Maryland/Greenebaum Cancer Center Baltimore, Maryland
University of Virginia Cancer Center Charlottesville, Virginia
VCU Massey Comprehensive Cancer Center Richmond, Virginia Site Public Contact - (CTOclinops@vcu.edu)

Prophylaxis With Direct-acting Antivirals for Kidney Transplantation From HCV-Infected Donors to Uninfected Recipients (PREVENT-HCV)

Christine Durand, MD - cdurand2@jhmi.edu

NCT05653232
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Inclusion Criteria:
* Participant meets the standard criteria for KT at local center. * Participant is able to understand and provide informed consent. * Participant is ≥ 18 years old.
Exclusion Criteria:
* Participant has active HCV infection (detectable HCV RNA) at time of screening. * Participant has cirrhosis or advanced liver fibrosis. * Participant's aspartate aminotransferase (AST) or ALT \> 2.5 times the upper limit of normal (ULN), within 60 days of screen. * Participant has human immunodeficiency virus infection (HIV), or active hepatitis B (HBV) infection. * Participant is unable to safely substitute or discontinue a medication that is contraindicated with the study medication. * Past or current medical problems, which may pose additional risks from participation in the study, interfere with the participant's ability to comply with study, or impact the quality of the data obtained from the study. * Participant is pregnant or breastfeeding.
OTHER: Prophylaxis (P2W), OTHER: Transmit and Treat (T&T)
HCV
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Icahn School of Medicine at Mount Sinai New York, New York Susan Lerner, MD - (Susan.Lerner@mountsinai.org)
Johns Hopkins University Baltimore, Maryland Christine Durand, MD - (cdurand2@jhmi.edu)
Loma Linda University Health Loma Linda, California Mina Rakoski, MD - (mrakoski@llu.edu)
NYU Langone Health New York, New York Aprajita Mattoo, MD - (Aprajita.Matoo@nyulangone.org)
University of California San Diego San Diego, California Saima Aslam, MD - (saslam@ucsd.edu)
University of Pittsburgh Medical Center Pittsburgh, Pennsylvania Fernanda Silveira, MD - (silvfd@upmc.edu)
University of Utah Medical Center Salt Lake City, Utah Miklos Molnar, MD, PhD - (miklos.molnar@hsc.utah.edu)
University of Wisconsin, Madison Madison, Wisconsin
Virginia Commonwealth University Richmond, Virginia Gaurav Gupta, MD - (gaurav.gupta@vcuhealth.org)

A Study of a New Way to Treat Children and Young Adults With a Brain Tumor Called NGGCT

ctrrecruit@vcu.edu

NCT04684368
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Inclusion Criteria:
* Patients must be \>= 3 years and \< 30 years at the time of study enrollment * Patients must be newly diagnosed with localized primary CNS NGGCT of the suprasellar and/or pineal region by pathology and/or serum or cerebrospinal fluid (CSF) elevation of AFP above institutional normal or \> 10 ng/mL or human chorionic gonadotropin (hCG) beta \> 100 mIU/mL as confirmed by Rapid Central Marker Screening Review on APEC14B1-CNS. Suprasellar, pineal and bifocal tumors are included. (CSF tumor markers and cytology must be within 31 days prior to enrollment and start of protocol therapy \[repeat if necessary\]. Serum tumor markers, AFP and hCGbeta must be within 7 days prior to enrollment and start of protocol therapy \[repeat if necessary\]). Basal ganglia or other primary sites are excluded * Patients with any of the following pathological elements are eligible: endodermal sinus (yolk sac), embryonal carcinoma, choriocarcinoma, malignant/immature teratoma and mixed germ cell tumor (GCT) (i.e., may include some pure germinoma) if malignant elements listed above are present. Patients with only mature teratoma are excluded. Patients with pure germinoma admixed with mature teratoma are excluded (would be eligible for pure germinoma protocols) * Patients must have a cranial MRI with and without gadolinium at diagnosis/prior to enrollment. If surgical resection is performed, patients must have pre-operative and post operative brain MRI with and without gadolinium. The post operative brain MRI should be obtained within 72 hours of surgery. If patient has a biopsy only, post-operative brain MRI is recommended but not required (within 31 days prior to study enrollment and start of protocol therapy ) * Patients must have a spine MRI with gadolinium obtained at diagnosis/prior to enrollment. Spine MRI with and without gadolinium is recommended (within 31 days prior to study enrollment and start of protocol therapy) * Lumbar CSF must be obtained prior to study enrollment unless medically contraindicated. If a patient undergoes surgery and lumbar CSF cytology cannot be obtained at the time of surgery, then it should be performed at least 10 days following surgery and prior to study enrollment. False positive cytology can occur within 10 days of surgery * Patients must have RAPID CENTRAL TUMOR MARKER REVIEW CSF tumor markers obtained prior to enrollment unless medically contraindicated. Ventricular CSF obtained at the time of CSF diversion procedure (if performed) is acceptable for tumor markers but lumbar CSF is preferred. In case CSF diversion and biopsy/surgery are combined, CSF tumor markers should be collected first * Peripheral absolute neutrophil count (ANC) \>= 1000/uL (within 7 days prior to enrollment) * Platelet count \>= 100,000/uL (transfusion independent) (within 7 days prior to enrollment) * Hemoglobin \>= 8.0 g/dL (may receive red blood cell \[RBC\] transfusions) (within 7 days prior to enrollment) * Creatinine clearance or radioisotope glomerular filtration rate (GFR) \>= 70 mL/min/1.73 m\^2 or a serum creatinine based on age/gender as follows (within 7 days prior to enrollment): * Age: Maximum serum creatinine (mg/dL) * 3 to \< 6 years: 0.8 (male), 0.8 (female) * 6 to \< 10 years: 1 (male), 1 (female) * 10 to \< 13 years: 1.2 (male), 1.2 (female) * 13 to \< 16 years: 1.5 (male), 1.4 (female) * \>= 16 years: male (1.7), 1.4 (female) * Total bilirubin =\< 1.5 x upper limit of normal (ULN) for age (within 7 days prior to enrollment) * Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase \[ALT\]) =\< 135 U/L (within 7 days prior to enrollment) * Note: For the purpose of this study, the ULN for SGPT (ALT) has been set to the value of 45 U/L * Central nervous system function defined as: * Patients with seizure disorder may be enrolled if on anticonvulsants and well controlled * Patients must not be in status epilepticus, coma or assisted ventilation prior to study enrollment * Protocol therapy must begin within 31 calendar days of definitive surgery or clinical diagnosis, whichever is later. If a biopsy only was performed, the biopsy date will be considered the date of definitive surgery. For patients who have a biopsy or incomplete resection at diagnosis followed by additional surgery, the date of the last resection will be considered the date of definitive surgery. * All patients and/or their parents or legal guardians must sign a written informed consent * All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met * NEUROCOGNITIVE FUNCTION AND QUALITY OF LIFE ASSESSMENT: * English-, Spanish-, or French- speaking * Note: Patients who speak a language other than English, Spanish, or French will be allowed to participate in ACNS2021 but will not complete the neurocognitive and quality of life assessments * No known history of neurodevelopmental disorder prior to diagnosis of NGGCT (e.g., Down syndrome, fragile X, William syndrome, intellectual disability). Patients with NF1 will be allowed to participate * Additional eligibility criteria for the COG Standardized Neuropsychological Battery only: must be at a site that has a psychologist to administer the battery * Note: If not eligible for the COG Standardized Battery, patients should still complete the Behavior Rating Inventory of Executive Function, Second Edition (BRIEF-2), Pediatric Quality of Life Inventory (PedsQL), Adaptive Behavior Assessment System Third Edition (ABAS-3), and Behavior Assessment System for Children, Third Edition (BASC-3) questionnaires
Exclusion Criteria:
* Patients with tumors located outside the ventricles (i.e., basal ganglia, thalamus) * Patients with only mature teratoma and non-elevated markers upon tumor sampling at diagnosis * Patients who have received any prior tumor-directed therapy for their diagnosis of NGGCT other than surgical intervention and corticosteroids * Patients with metastatic disease (i.e., MRI evaluation, lumbar CSF cytology or intraoperative evidence of dissemination) * Female patients who are pregnant, since fetal toxicities and teratogenic effects have been noted for several of the study drugs * Note: Serum and urine pregnancy tests may be falsely positive due to HCGbeta-secreting germ cell tumors. Ensure the patient is not pregnant by institutional standards * Lactating females who plan to breastfeed their infants * Sexually active patients of reproductive potential who have not agreed to use an effective contraceptive method for the duration of their study participation
PROCEDURE: Biospecimen Collection, DRUG: Carboplatin, DRUG: Etoposide, BIOLOGICAL: Filgrastim, DRUG: Ifosfamide, PROCEDURE: Magnetic Resonance Imaging, DRUG: Mesna, BIOLOGICAL: Pegfilgrastim, PROCEDURE: Peripheral Blood Stem Cell Transplantation, OTHER: Questionnaire Administration, RADIATION: Radiation Therapy, RADIATION: Radiation Therapy, PROCEDURE: Second-Look Surgery, DRUG: Thiotepa
Central Nervous System Nongerminomatous Germ Cell Tumor, Choriocarcinoma, Embryonal Carcinoma, Immature Teratoma, Malignant Teratoma, Mixed Germ Cell Tumor, Pineal Region Germ Cell Tumor, Pineal Region Immature Teratoma, Pineal Region Yolk Sac Tumor, Suprasellar Germ Cell Tumor
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Albany Medical Center Albany, New York
Alberta Children's Hospital Calgary, Alberta Site Public Contact - (research4kids@ucalgary.ca)
Alfred I duPont Hospital for Children Wilmington, Delaware Site Public Contact - (Allison.bruce@nemours.org)
Alliance for Childhood Diseases/Cure 4 the Kids Foundation Las Vegas, Nevada
Arkansas Children's Hospital Little Rock, Arkansas
Arnold Palmer Hospital for Children Orlando, Florida Site Public Contact - (Jennifer.spinelli@orlandohealth.com)
BI-LO Charities Children's Cancer Center Greenville, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Banner Children's at Desert Mesa, Arizona
Banner University Medical Center - Tucson Tucson, Arizona Site Public Contact - (UACC-IIT@uacc.arizona.edu)
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center Houston, Texas Site Public Contact - (burton@bcm.edu)
Blank Children's Hospital Des Moines, Iowa Site Public Contact - (samantha.mallory@unitypoint.org)
British Columbia Children's Hospital Vancouver, British Columbia
C S Mott Children's Hospital Ann Arbor, Michigan
CHU de Quebec-Centre Hospitalier de l'Universite Laval (CHUL) Québec, Site Public Contact - (rechclinique@crchudequebec.ulaval.ca)
Cancer Care Specialists - Reno Reno, Nevada
CancerCare Manitoba Winnipeg, Manitoba Site Public Contact - (ctu_web@cancercare.mb.ca)
Cardinal Glennon Children's Medical Center St Louis, Missouri
Carilion Children's Roanoke, Virginia Site Public Contact - (wpmccarty@carilionclinic.org)
Carolinas Medical Center/Levine Cancer Institute Charlotte, North Carolina
Cedars Sinai Medical Center Los Angeles, California
Centre Hospitalier Universitaire Sainte-Justine Montreal, Quebec Site Public Contact - (yvan.samson@umontreal.ca)
Centre Hospitalier Universitaire de Sherbrooke-Fleurimont Sherbrooke, Quebec Site Public Contact - (crcinformation.chus@ssss.gouv.qc.ca)
Children's Healthcare of Atlanta - Arthur M Blank Hospital Atlanta, Georgia Site Public Contact - (Olivia.Floyd@choa.org)
Children's Hospital Colorado Aurora, Colorado Site Public Contact - (josh.b.gordon@nsmtp.kp.org)
Children's Hospital Los Angeles Los Angeles, California
Children's Hospital Medical Center Of Akron Akron, Ohio
Children's Hospital and Medical Center of Omaha Omaha, Nebraska
Children's Hospital of Alabama Birmingham, Alabama
Children's Hospital of Michigan Detroit, Michigan Site Public Contact - (helpdesk@childrensoncologygroup.org)
Children's Hospital of Orange County Orange, California Site Public Contact - (oncresearch@choc.org)
Children's Hospital of Pittsburgh of UPMC Pittsburgh, Pennsylvania Site Public Contact - (jean.tersak@chp.edu)
Children's Hospital of San Antonio San Antonio, Texas Site Public Contact - (bridget.medina@christushealth.org)
Children's Hospital of the King's Daughters Norfolk, Virginia Site Public Contact - (CCBDCresearch@chkd.org)
Children's Hospitals and Clinics of Minnesota - Minneapolis Minneapolis, Minnesota Site Public Contact - (pauline.mitby@childrensmn.org)
Children's Mercy Hospitals and Clinics Kansas City, Missouri Site Public Contact - (COGResearchGroup@cmh.edu)
Children's National Medical Center Washington D.C., District of Columbia Site Public Contact - (OncCRC_OnCall@childrensnational.org)
Christchurch Hospital Christchurch,
Cincinnati Children's Hospital Medical Center Cincinnati, Ohio Site Public Contact - (cancer@cchmc.org)
Cleveland Clinic Foundation Cleveland, Ohio
Connecticut Children's Medical Center Hartford, Connecticut
Cook Children's Medical Center Fort Worth, Texas Site Public Contact - (CookChildrensResearch@cookchildrens.org)
Corewell Health Children's Royal Oak, Michigan
Corewell Health Grand Rapids Hospitals - Butterworth Hospital Grand Rapids, Michigan
Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital Grand Rapids, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Dana-Farber Cancer Institute Boston, Massachusetts
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center Lebanon, New Hampshire Site Public Contact - (cancer.research.nurse@dartmouth.edu)
Dayton Children's Hospital Dayton, Ohio
Dell Children's Medical Center of Central Texas Austin, Texas Site Public Contact - (TXAUS-DL-SFCHemonc.research@ascension.org)
Driscoll Children's Hospital Corpus Christi, Texas Site Public Contact - (Crystal.DeLosSantos@dchstx.org)
Duke University Medical Center Durham, North Carolina
East Carolina University Greenville, North Carolina Site Public Contact - (eubankss@ecu.edu)
Eastern Maine Medical Center Bangor, Maine
El Paso Children's Hospital El Paso, Texas Site Public Contact - (ranjan.bista@ttuhsc.edu)
Geisinger Medical Center Danville, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Golisano Children's Hospital of Southwest Florida Fort Myers, Florida Site Public Contact - (molly.arnstrom@leehealth.org)
Hackensack University Medical Center Hackensack, New Jersey
Hospital for Sick Children Toronto, Ontario
IWK Health Centre Halifax, Nova Scotia Site Public Contact - (Research@iwk.nshealth.ca)
Johns Hopkins All Children's Hospital St. Petersburg, Florida Site Public Contact - (Ashley.Repp@jhmi.edu)
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore, Maryland Site Public Contact - (jhcccro@jhmi.edu)
Kaiser Permanente Downey Medical Center Downey, California
Kaiser Permanente Los Angeles Medical Center Los Angeles, California
Kaiser Permanente-Oakland Oakland, California Site Public Contact - (Kpoct@kp.org)
Kapiolani Medical Center for Women and Children Honolulu, Hawaii
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York, New York Site Public Contact - (CancerTrials@nyulangone.org)
Legacy Emanuel Children's Hospital Portland, Oregon
Lehigh Valley Hospital-Cedar Crest Allentown, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Loma Linda University Medical Center Murrieta, California
Loyola University Medical Center Maywood, Illinois
Lucile Packard Children's Hospital Stanford University Palo Alto, California Site Public Contact - (ccto-office@stanford.edu)
Lurie Children's Hospital-Chicago Chicago, Illinois
M D Anderson Cancer Center Houston, Texas Najat C. Daw - (ndaw@mdanderson.org)
Madigan Army Medical Center Tacoma, Washington Site Public Contact - (melissa.a.forouhar.mil@health.mil)
Maimonides Medical Center Brooklyn, New York
Maine Children's Cancer Program Scarborough, Maine Site Public Contact - (clinicalresearch@mainehealth.org)
Marshfield Medical Center-Marshfield Marshfield, Wisconsin
Mary Bridge Children's Hospital and Health Center Tacoma, Washington Site Public Contact - (research@multicare.org)
Massachusetts General Hospital Cancer Center Boston, Massachusetts
Mayo Clinic in Rochester Rochester, Minnesota
McMaster Children's Hospital at Hamilton Health Sciences Hamilton, Ontario
Medical City Dallas Hospital Dallas, Texas
Medical University of South Carolina Charleston, South Carolina Site Public Contact - (hcc-clinical-trials@musc.edu)
Memorial Sloan Kettering Cancer Center New York, New York
Mercy Hospital Saint Louis St Louis, Missouri
Methodist Children's Hospital of South Texas San Antonio, Texas Site Public Contact - (Vinod.GidvaniDiaz@hcahealthcare.com)
Michigan State University East Lansing, Michigan
Miller Children's and Women's Hospital Long Beach Long Beach, California
Montefiore Medical Center - Moses Campus The Bronx, New York Site Public Contact - (eskwak@montefiore.org)
Montefiore Medical Center-Einstein Campus The Bronx, New York
Morristown Medical Center Morristown, New Jersey
Nationwide Children's Hospital Columbus, Ohio Site Public Contact - (Melinda.Triplet@nationwidechildrens.org)
Nemours Children's Clinic - Pensacola Pensacola, Florida Site Public Contact - (helpdesk@childrensoncologygroup.org)
Nemours Children's Clinic-Jacksonville Jacksonville, Florida Site Public Contact - (Allison.bruce@nemours.org)
Nemours Children's Hospital Orlando, Florida Site Public Contact - (Allison.bruce@nemours.org)
New York Medical College Valhalla, New York
Newark Beth Israel Medical Center Newark, New Jersey
Nicklaus Children's Hospital Miami, Florida
Norton Children's Hospital Louisville, Kentucky Site Public Contact - (CancerResource@nortonhealthcare.org)
Ochsner Medical Center Jefferson New Orleans, Louisiana Site Public Contact - (Elisemarie.curry@ochsner.org)
Oncology Las Vegas - Henderson Henderson, Nevada
Oregon Health and Science University Portland, Oregon Site Public Contact - (trials@ohsu.edu)
Penn State Children's Hospital Hershey, Pennsylvania
Perth Children's Hospital Perth, Western Australia Site Public Contact - (helpdesk@childrensoncologygroup.org)
Phoenix Childrens Hospital Phoenix, Arizona
Primary Children's Hospital Salt Lake City, Utah
Prisma Health Cancer Institute - Faris Greenville, South Carolina
Prisma Health Richland Hospital Columbia, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
ProMedica Flower Hospital Sylvania, Ohio
ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital Toledo, Ohio Site Public Contact - (PCIOncResearch@promedica.org)
Providence Alaska Medical Center Anchorage, Alaska Site Public Contact - (AKPAMC.OncologyResearchSupport@providence.org)
Providence Sacred Heart Medical Center and Children's Hospital Spokane, Washington Site Public Contact - (HopeBeginsHere@providence.org)
Queensland Children's Hospital South Brisbane, Queensland
Rady Children's Hospital - San Diego San Diego, California
Rainbow Babies and Childrens Hospital Cleveland, Ohio
Renown Regional Medical Center Reno, Nevada Site Public Contact - (research@sncrf.org)
Rhode Island Hospital Providence, Rhode Island
Riley Hospital for Children Indianapolis, Indiana Sandeep Batra - (batras@iu.edu)
Royal Children's Hospital Parkville, Victoria Site Public Contact - (Jordan.Hansford@rch.org.au)
Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital New Brunswick, New Jersey
Sacred Heart Hospital Pensacola, Florida
Saint Christopher's Hospital for Children Philadelphia, Pennsylvania
Saint Joseph's Hospital/Children's Hospital-Tampa Tampa, Florida Site Public Contact - (jennifer.manns@baycare.org)
Saint Joseph's Regional Medical Center Paterson, New Jersey Site Public Contact - (HallL@sjhmc.org)
Saint Jude Children's Research Hospital Memphis, Tennessee Site Public Contact - (referralinfo@stjude.org)
Saint Jude Midwest Affiliate Peoria, Illinois
Saint Luke's Cancer Institute - Boise Boise, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Peter's University Hospital New Brunswick, New Jersey Site Public Contact - (kcovert@saintpetersuh.com)
Sanford Broadway Medical Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford USD Medical Center - Sioux Falls Sioux Falls, South Dakota Site Public Contact - (OncologyClinicalTrialsSF@SanfordHealth.org)
Scott and White Memorial Hospital Temple, Texas
Seattle Children's Hospital Seattle, Washington
Sinai Hospital of Baltimore Baltimore, Maryland
State University of New York Upstate Medical University Syracuse, New York
Stony Brook University Medical Center Stony Brook, New York
Sydney Children's Hospital Randwick, New South Wales
The Children's Hospital at TriStar Centennial Nashville, Tennessee
The Children's Hospital at Westmead Westmead, New South Wales
The Montreal Children's Hospital of the MUHC Montreal, Quebec Site Public Contact - (info@thechildren.com)
The Steven and Alexandra Cohen Children's Medical Center of New York New Hyde Park, New York
UCSF Medical Center-Mission Bay San Francisco, California Site Public Contact - (cancertrials@ucsf.edu)
UF Health Cancer Institute - Gainesville Gainesville, Florida Site Public Contact - (cancer-center@ufl.edu)
UT Southwestern/Simmons Cancer Center-Dallas Dallas, Texas Daniel C. Bowers - (Daniel.Bowers@utsouthwestern.edu)
University of Alberta Hospital Edmonton, Alberta Site Public Contact - (pedsoncologyresearch@ahs.ca)
University of Arizona Cancer Center-North Campus Tucson, Arizona
University of Chicago Comprehensive Cancer Center Chicago, Illinois Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
University of Illinois Chicago, Illinois
University of Iowa/Holden Comprehensive Cancer Center Iowa City, Iowa
University of Kentucky/Markey Cancer Center Lexington, Kentucky
University of Miami Miller School of Medicine-Sylvester Cancer Center Miami, Florida
University of Mississippi Medical Center Jackson, Mississippi
University of Missouri Children's Hospital Columbia, Missouri Site Public Contact - (snwq62@health.missouri.edu)
University of Nebraska Medical Center Omaha, Nebraska Site Public Contact - (unmcrsa@unmc.edu)
University of Oklahoma Health Sciences Center Oklahoma City, Oklahoma Site Public Contact - (ou-clinical-trials@ouhsc.edu)
University of Rochester Rochester, New York
University of Texas Health Science Center at San Antonio San Antonio, Texas Site Public Contact - (phoresearchoffice@uthscsa.edu)
University of Vermont and State Agricultural College Burlington, Vermont Site Public Contact - (rpo@uvm.edu)
University of Virginia Cancer Center Charlottesville, Virginia Site Public Contact - (uvacancertrials@hscmail.mcc.virginia.edu)
University of Wisconsin Carbone Cancer Center - University Hospital Madison, Wisconsin Site Public Contact - (clinicaltrials@cancer.wisc.edu)
VCU Massey Comprehensive Cancer Center Richmond, Virginia Site Public Contact - (CTOclinops@vcu.edu)
Valley Children's Hospital Madera, California Site Public Contact - (Research@valleychildrens.org)
Vanderbilt University/Ingram Cancer Center Nashville, Tennessee
Wake Forest University Health Sciences Winston-Salem, North Carolina
Washington University School of Medicine St Louis, Missouri Site Public Contact - (info@siteman.wustl.edu)
West Virginia University Healthcare Morgantown, West Virginia Site Public Contact - (cancertrialsinfo@hsc.wvu.edu)
Yale University New Haven, Connecticut Site Public Contact - (canceranswers@yale.edu)

The Pediatric Acute Leukemia (PedAL) Screening Trial - A Study to Test Bone Marrow and Blood in Children With Leukemia That Has Come Back After Treatment or Is Difficult to Treat - A Leukemia & Lymphoma Society and Children's Oncology Group Study

ctrrecruit@vcu.edu

NCT04726241
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Inclusion Criteria:
* Patients must be less than 22 years of age at the time of study enrollment * Patient must have one of the following at the time of study enrollment: * Patient has known or suspected relapsed/refractory (including primary refractory) AML as defined in protocol * This includes isolated myeloid sarcoma * Patient has known or suspected relapsed/refractory (including primary refractory) myeloid leukemia of Down syndrome (ML-DS) * Patient has known or suspected relapsed ALL as defined in protocol that meets one of the following criteria: * Second or greater B-ALL medullary relapse, excluding KMT2Ar * Any first or greater B-ALL medullary relapse involving KMT2Ar * Any first or greater T-ALL medullary relapse with or without KMT2Ar * Patient has known or suspected relapsed/refractory (including primary refractory) mixed phenotype acute leukemia (MPAL) as defined in protocol * Patient has known or suspected de novo or relapsed/refractory (including primary refractory) treatment-related AML (t-AML) * Patient has known or suspected de novo or relapsed/refractory (including primary refractory) myelodysplastic syndrome (MDS) or treatment-related myelodysplastic syndrome (t-MDS) * Note: Relapsed/refractory disease includes stable disease, progressive disease, and disease relapse. * Patient has known or suspected de novo or relapsed/refractory (including primary refractory) juvenile myelomonocytic leukemia (JMML) * Note: Relapsed/refractory disease includes stable disease, progressive disease, and disease relapse. * All patients and/or their parents or legal guardians must sign a written informed consent * All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met
PROCEDURE: Biospecimen Collection
Acute Lymphoblastic Leukemia, Acute Myeloid Leukemia, Acute Myeloid Leukemia Post Cytotoxic Therapy, Juvenile Myelomonocytic Leukemia, Mixed Phenotype Acute Leukemia, Myelodysplastic Syndrome, Myelodysplastic Syndrome Post Cytotoxic Therapy, Myeloid Leukemia Associated With Down Syndrome
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Study Locations

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Location Contacts
Advocate Children's Hospital-Oak Lawn Oak Lawn, Illinois
Advocate Children's Hospital-Park Ridge Park Ridge, Illinois Site Public Contact - (helpdesk@childrensoncologygroup.org)
Albany Medical Center Albany, New York
Alberta Children's Hospital Calgary, Alberta Site Public Contact - (research4kids@ucalgary.ca)
Alfred I duPont Hospital for Children Wilmington, Delaware Site Public Contact - (Allison.bruce@nemours.org)
Alliance for Childhood Diseases/Cure 4 the Kids Foundation Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
Arkansas Children's Hospital Little Rock, Arkansas
Arnold Palmer Hospital for Children Orlando, Florida Site Public Contact - (Jennifer.spinelli@orlandohealth.com)
Ascension Saint Vincent Indianapolis Hospital Indianapolis, Indiana Site Public Contact - (research@stvincent.org)
BI-LO Charities Children's Cancer Center Greenville, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Banner Children's at Desert Mesa, Arizona
Banner University Medical Center - Tucson Tucson, Arizona Site Public Contact - (UACC-IIT@uacc.arizona.edu)
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center Houston, Texas Site Public Contact - (burton@bcm.edu)
Blank Children's Hospital Des Moines, Iowa Site Public Contact - (samantha.mallory@unitypoint.org)
British Columbia Children's Hospital Vancouver, British Columbia
Bronson Methodist Hospital Kalamazoo, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Broward Health Medical Center Fort Lauderdale, Florida Site Public Contact - (Allison.bruce@nemours.org)
C S Mott Children's Hospital Ann Arbor, Michigan
CHU de Quebec-Centre Hospitalier de l'Universite Laval (CHUL) Québec, Site Public Contact - (rechclinique@crchudequebec.ulaval.ca)
CancerCare Manitoba Winnipeg, Manitoba Site Public Contact - (ctu_web@cancercare.mb.ca)
Cardinal Glennon Children's Medical Center St Louis, Missouri
Carilion Children's Roanoke, Virginia Site Public Contact - (wpmccarty@carilionclinic.org)
Carolinas Medical Center/Levine Cancer Institute Charlotte, North Carolina
Centre Hospitalier Universitaire Sainte-Justine Montreal, Quebec Site Public Contact - (yvan.samson@umontreal.ca)
Centre Hospitalier Universitaire de Sherbrooke-Fleurimont Sherbrooke, Quebec Site Public Contact - (crcinformation.chus@ssss.gouv.qc.ca)
Children's Healthcare of Atlanta - Arthur M Blank Hospital Atlanta, Georgia Site Public Contact - (Olivia.Floyd@choa.org)
Children's Hospital London, Ontario
Children's Hospital Colorado Aurora, Colorado Site Public Contact - (josh.b.gordon@nsmtp.kp.org)
Children's Hospital Los Angeles Los Angeles, California
Children's Hospital Medical Center Of Akron Akron, Ohio
Children's Hospital New Orleans New Orleans, Louisiana
Children's Hospital Of Eastern Ontario Ottawa, Ontario
Children's Hospital and Medical Center of Omaha Omaha, Nebraska
Children's Hospital of Alabama Birmingham, Alabama Site Public Contact - (oncologyresearch@peds.uab.edu)
Children's Hospital of Michigan Detroit, Michigan Site Public Contact - (helpdesk@childrensoncologygroup.org)
Children's Hospital of Orange County Orange, California Site Public Contact - (oncresearch@choc.org)
Children's Hospital of Philadelphia Philadelphia, Pennsylvania Site Public Contact - (CancerTrials@email.chop.edu)
Children's Hospital of Pittsburgh of UPMC Pittsburgh, Pennsylvania Site Public Contact - (jean.tersak@chp.edu)
Children's Hospital of San Antonio San Antonio, Texas Site Public Contact - (bridget.medina@christushealth.org)
Children's Hospital of the King's Daughters Norfolk, Virginia Site Public Contact - (CCBDCresearch@chkd.org)
Children's Hospitals and Clinics of Minnesota - Minneapolis Minneapolis, Minnesota Site Public Contact - (pauline.mitby@childrensmn.org)
Children's Mercy Hospitals and Clinics Kansas City, Missouri Site Public Contact - (COGResearchGroup@cmh.edu)
Children's National Medical Center Washington D.C., District of Columbia Site Public Contact - (OncCRC_OnCall@childrensnational.org)
Christchurch Hospital Christchurch,
Cincinnati Children's Hospital Medical Center Cincinnati, Ohio Site Public Contact - (cancer@cchmc.org)
Cleveland Clinic Foundation Cleveland, Ohio
Connecticut Children's Medical Center Hartford, Connecticut
Cook Children's Medical Center Fort Worth, Texas Site Public Contact - (CookChildrensResearch@cookchildrens.org)
Corewell Health Children's Royal Oak, Michigan
Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital Grand Rapids, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Covenant Children's Hospital Lubbock, Texas Site Public Contact - (mbisbee@providence.org)
Dana-Farber Cancer Institute Boston, Massachusetts
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center Lebanon, New Hampshire Site Public Contact - (cancer.research.nurse@dartmouth.edu)
Dayton Children's Hospital Dayton, Ohio
Dell Children's Medical Center of Central Texas Austin, Texas Site Public Contact - (TXAUS-DL-SFCHemonc.research@ascension.org)
Driscoll Children's Hospital Corpus Christi, Texas Site Public Contact - (Crystal.DeLosSantos@dchstx.org)
Duke University Medical Center Durham, North Carolina
East Carolina University Greenville, North Carolina Site Public Contact - (eubankss@ecu.edu)
East Tennessee Childrens Hospital Knoxville, Tennessee
Eastern Maine Medical Center Bangor, Maine
El Paso Children's Hospital El Paso, Texas Site Public Contact - (ranjan.bista@ttuhsc.edu)
Geisinger Medical Center Danville, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Golisano Children's Hospital of Southwest Florida Fort Myers, Florida Site Public Contact - (molly.arnstrom@leehealth.org)
HIMA San Pablo Oncologic Hospital Caguas,
Hackensack University Medical Center Hackensack, New Jersey
Hospital for Sick Children Toronto, Ontario Site Public Contact - (ask.CRS@sickkids.ca)
IWK Health Centre Halifax, Nova Scotia Site Public Contact - (Research@iwk.nshealth.ca)
Inova Fairfax Hospital Falls Church, Virginia Site Public Contact - (Stephanie.VanBebber@inova.org)
Jersey Shore Medical Center Neptune City, New Jersey
Johns Hopkins All Children's Hospital St. Petersburg, Florida Site Public Contact - (Ashley.Repp@jhmi.edu)
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore, Maryland Site Public Contact - (jhcccro@jhmi.edu)
Kaiser Permanente Downey Medical Center Downey, California
Kaiser Permanente-Oakland Oakland, California Site Public Contact - (Kpoct@kp.org)
Kapiolani Medical Center for Women and Children Honolulu, Hawaii
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York, New York Site Public Contact - (CancerTrials@nyulangone.org)
Legacy Emanuel Children's Hospital Portland, Oregon
Lehigh Valley Hospital-Cedar Crest Allentown, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Loma Linda University Medical Center Murrieta, California
Loyola University Medical Center Maywood, Illinois
Lucile Packard Children's Hospital Stanford University Palo Alto, California Site Public Contact - (ccto-office@stanford.edu)
Lurie Children's Hospital-Chicago Chicago, Illinois
M D Anderson Cancer Center Houston, Texas Site Public Contact - (askmdanderson@mdanderson.org)
Madigan Army Medical Center Tacoma, Washington Site Public Contact - (melissa.a.forouhar.mil@health.mil)
Maimonides Medical Center Brooklyn, New York
Maine Children's Cancer Program Scarborough, Maine Site Public Contact - (clinicalresearch@mainehealth.org)
Marshfield Medical Center-Marshfield Marshfield, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Mary Bridge Children's Hospital and Health Center Tacoma, Washington Site Public Contact - (research@multicare.org)
Mayo Clinic in Rochester Rochester, Minnesota
MedStar Georgetown University Hospital Washington D.C., District of Columbia
Medical City Dallas Hospital Dallas, Texas
Medical University of South Carolina Charleston, South Carolina Site Public Contact - (hcc-clinical-trials@musc.edu)
Memorial Health University Medical Center Savannah, Georgia Site Public Contact - (Lorraine.OHara@hcahealthcare.com)
Memorial Regional Hospital/Joe DiMaggio Children's Hospital Hollywood, Florida Site Public Contact - (OHR@mhs.net)
Memorial Sloan Kettering Cancer Center New York, New York
Mercy Hospital Saint Louis St Louis, Missouri
Methodist Children's Hospital of South Texas San Antonio, Texas Site Public Contact - (Vinod.GidvaniDiaz@hcahealthcare.com)
Michigan State University East Lansing, Michigan
Miller Children's and Women's Hospital Long Beach Long Beach, California
Mission Hospital Asheville, North Carolina Site Public Contact - (NCDV.ResearchRegulatory@HCAHealthcare.com)
Montefiore Medical Center - Moses Campus The Bronx, New York Site Public Contact - (eskwak@montefiore.org)
Morristown Medical Center Morristown, New Jersey
NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center New York, New York Site Public Contact - (cancerclinicaltrials@cumc.columbia.edu)
NYU Langone Hospital - Long Island Mineola, New York Site Public Contact - (cancertrials@nyulangone.org)
Nationwide Children's Hospital Columbus, Ohio Site Public Contact - (Melinda.Triplet@nationwidechildrens.org)
Nemours Children's Clinic - Pensacola Pensacola, Florida Site Public Contact - (helpdesk@childrensoncologygroup.org)
Nemours Children's Clinic-Jacksonville Jacksonville, Florida Site Public Contact - (Allison.bruce@nemours.org)
Nemours Children's Hospital Orlando, Florida Site Public Contact - (Allison.bruce@nemours.org)
New York Medical College Valhalla, New York
Nicklaus Children's Hospital Miami, Florida
Norton Children's Hospital Louisville, Kentucky Site Public Contact - (CancerResource@nortonhealthcare.org)
Novant Health Presbyterian Medical Center Charlotte, North Carolina Site Public Contact - (kashah@novanthealth.org)
Ochsner Medical Center Jefferson New Orleans, Louisiana Site Public Contact - (Elisemarie.curry@ochsner.org)
Oregon Health and Science University Portland, Oregon Site Public Contact - (trials@ohsu.edu)
Penn State Children's Hospital Hershey, Pennsylvania
Perth Children's Hospital Perth, Western Australia Site Public Contact - (helpdesk@childrensoncologygroup.org)
Phoenix Childrens Hospital Phoenix, Arizona
Primary Children's Hospital Salt Lake City, Utah
Prisma Health Richland Hospital Columbia, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital Toledo, Ohio Site Public Contact - (PCIOncResearch@promedica.org)
Providence Alaska Medical Center Anchorage, Alaska Site Public Contact - (AKPAMC.OncologyResearchSupport@providence.org)
Providence Sacred Heart Medical Center and Children's Hospital Spokane, Washington Site Public Contact - (HopeBeginsHere@providence.org)
Queensland Children's Hospital South Brisbane, Queensland
Rady Children's Hospital - San Diego San Diego, California
Rainbow Babies and Childrens Hospital Cleveland, Ohio
Renown Regional Medical Center Reno, Nevada Site Public Contact - (research@sncrf.org)
Rhode Island Hospital Providence, Rhode Island
Riley Hospital for Children Indianapolis, Indiana
Rocky Mountain Hospital for Children-Presbyterian Saint Luke's Medical Center Denver, Colorado Site Public Contact - (PSGResearchSharedMailbox@HCAHealthcare.com)
Royal Children's Hospital Parkville, Victoria Site Public Contact - (Jordan.Hansford@rch.org.au)
Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital New Brunswick, New Jersey
Sacred Heart Hospital Pensacola, Florida
Saint Christopher's Hospital for Children Philadelphia, Pennsylvania
Saint Joseph's Hospital/Children's Hospital-Tampa Tampa, Florida Site Public Contact - (jennifer.manns@baycare.org)
Saint Joseph's Regional Medical Center Paterson, New Jersey Site Public Contact - (HallL@sjhmc.org)
Saint Jude Children's Research Hospital Memphis, Tennessee Site Public Contact - (referralinfo@stjude.org)
Saint Jude Midwest Affiliate Peoria, Illinois
Saint Luke's Cancer Institute - Boise Boise, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Mary's Medical Center West Palm Beach, Florida
Saint Peter's University Hospital New Brunswick, New Jersey Site Public Contact - (kcovert@saintpetersuh.com)
Sanford Broadway Medical Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford USD Medical Center - Sioux Falls Sioux Falls, South Dakota Site Public Contact - (OncologyClinicalTrialsSF@SanfordHealth.org)
Seattle Children's Hospital Seattle, Washington
Sinai Hospital of Baltimore Baltimore, Maryland
Southern Illinois University School of Medicine Springfield, Illinois
Starship Children's Hospital Grafton, Auckland
State University of New York Upstate Medical University Syracuse, New York
Stony Brook University Medical Center Stony Brook, New York
Summerlin Hospital Medical Center Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
The Children's Hospital at TriStar Centennial Nashville, Tennessee
The Children's Hospital at Westmead Westmead, New South Wales
The Montreal Children's Hospital of the MUHC Montreal, Quebec Site Public Contact - (info@thechildren.com)
The Steven and Alexandra Cohen Children's Medical Center of New York New Hyde Park, New York
UCSF Benioff Children's Hospital Oakland Oakland, California Site Public Contact - (PedOncRschOAK@ucsf.edu)
UCSF Medical Center-Mission Bay San Francisco, California Site Public Contact - (cancertrials@ucsf.edu)
UF Health Cancer Institute - Gainesville Gainesville, Florida
UMC Cancer Center / UMC Health System Lubbock, Texas
UNC Lineberger Comprehensive Cancer Center Chapel Hill, North Carolina Site Public Contact - (cancerclinicaltrials@med.unc.edu)
USA Health Strada Patient Care Center Mobile, Alabama
UT Southwestern/Simmons Cancer Center-Dallas Dallas, Texas Site Public Contact - (canceranswerline@UTSouthwestern.edu)
University of Alberta Hospital Edmonton, Alberta Site Public Contact - (pedsoncologyresearch@ahs.ca)
University of Chicago Comprehensive Cancer Center Chicago, Illinois Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
University of Illinois Chicago, Illinois
University of Iowa/Holden Comprehensive Cancer Center Iowa City, Iowa
University of Kentucky/Markey Cancer Center Lexington, Kentucky
University of Minnesota/Masonic Cancer Center Minneapolis, Minnesota
University of Mississippi Medical Center Jackson, Mississippi
University of Missouri Children's Hospital Columbia, Missouri Site Public Contact - (snwq62@health.missouri.edu)
University of Nebraska Medical Center Omaha, Nebraska Site Public Contact - (unmcrsa@unmc.edu)
University of New Mexico Cancer Center Albuquerque, New Mexico Site Public Contact - (HSC-ClinicalTrialInfo@salud.unm.edu)
University of Oklahoma Health Sciences Center Oklahoma City, Oklahoma Site Public Contact - (ou-clinical-trials@ouhsc.edu)
University of Rochester Rochester, New York
University of Texas Health Science Center at San Antonio San Antonio, Texas Site Public Contact - (phoresearchoffice@uthscsa.edu)
University of Virginia Cancer Center Charlottesville, Virginia Site Public Contact - (uvacancertrials@hscmail.mcc.virginia.edu)
University of Wisconsin Carbone Cancer Center - University Hospital Madison, Wisconsin Kenneth B. De Santes - (kbdesantes@pediatrics.wisc.edu)
VCU Massey Comprehensive Cancer Center Richmond, Virginia Site Public Contact - (CTOclinops@vcu.edu)
Valley Children's Hospital Madera, California Site Public Contact - (Research@valleychildrens.org)
Vanderbilt University/Ingram Cancer Center Nashville, Tennessee
Wake Forest University Health Sciences Winston-Salem, North Carolina
Walter Reed National Military Medical Center Bethesda, Maryland
Washington University School of Medicine St Louis, Missouri Site Public Contact - (info@siteman.wustl.edu)
West Virginia University Healthcare Morgantown, West Virginia Site Public Contact - (cancertrialsinfo@hsc.wvu.edu)
Yale University New Haven, Connecticut Site Public Contact - (canceranswers@yale.edu)

Anticoagulation in ICH Survivors for Stroke Prevention and Recovery (ASPIRE)

Kevin N Sheth, MD - kevin.sheth@yale.edu

NCT03907046
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Inclusion Criteria:
* Age at least 18 years * Intracerebral hemorrhage (ICH) (including primary intraventricular hemorrhage) confirmed by brain CT or MRI * Can be randomized within 14-180 days after ICH onset * Non-valvular AF (defined as atrial fibrillation or atrial flutter), documented by electrocardiography or a physician-confirmed history of prior AF * Provision of signed and dated informed consent form by patient or legally authorized representative * For females of reproductive potential: use of highly effective contraception
Exclusion Criteria:
* Index event is hemorrhagic transformation of a brain infarction or hemorrhage into a tumor * History of earlier ICH within 12 months preceding index event * Active infective endocarditis * Clear indication for anticoagulant drugs (e.g., requires anticoagulation for deep vein thrombosis or pulmonary embolism) or antiplatelet drugs (e.g., requires aspirin or clopidogrel for recent coronary stent). * Previous or planned left atrial appendage closure * Clinically significant bleeding diathesis * Serum creatinine ≥2.5 mg/dL * Active hepatitis or hepatic insufficiency with Child-Pugh score B or C * Anemia (hemoglobin \<8 g/dL) or thrombocytopenia (\<100 x 10\^9/L) that is chronic in the judgment of the investigator * Pregnant or breastfeeding * Known allergy to aspirin or apixaban * Concomitant participation in a competing trial * Considered by the investigator to have a condition that precludes safe or active participation in the trial * Persistent, uncontrolled systolic blood pressure (≥180 mm Hg) * ICH caused by an arteriovenous malformation (AVM) that has not yet been secured
DRUG: Apixaban, DRUG: Aspirin
Intracerebral Hemorrhage, Atrial Fibrillation
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Study Locations

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Location Contacts
Abbott Northwestern Hospital Minneapolis, Minnesota
Arrowhead Regional Medical Center Colton, California
Ascension Sacred Heart Pensacola Pensacola, Florida
Ascension St. John Medical Center Tulsa, Oklahoma
Augusta University Medical Center Augusta, Georgia
Avera Research Institute Sioux Falls, South Dakota
Banner University Medical Center Phoenix, Arizona
Baptist Health Lexington Lexington, Kentucky
Barnes Jewish Hospital St Louis, Missouri
Baylor College of Medicine Medical Center Houston, Texas
Baystate Medical Center Springfield, Massachusetts
Beth Israel Deaconess Medical Center Boston, Massachusetts
Bon Secours St. Mary's Hospital Richmond, Virginia
Boston Medical Center Boston, Massachusetts
Broward Health Medical Center Fort Lauderdale, Florida
Buffalo General Medical Center Buffalo, New York
Burke Rehabilitation Center White Plains, New York
Capital Health Regional Medical Center Pennington, New Jersey
Carolinas Medical Center Charlotte, North Carolina
Cedars-Sinai Medical Center Beverly Hills, California
Central DuPage Hospital Winfield, Illinois
Chandler Regional Medical Center Chandler, Arizona
Cleveland Clinic Cleveland, Ohio
Cleveland Clinic Akron General Akron, Ohio
Cleveland Clinic Tradition Hospital Port Saint Lucie, Florida
Community Regional Medical Center of Fresno Fresno, California
Cooperman Barnabas Medical Center West Orange, New Jersey
Cox Medical Center South Springfield, Missouri
Danbury Hospital Danbury, Connecticut
Desert Regional Medical Center Palm Springs, California
Doctors Medical Center Modesto, Modesto, CA Modesto, California
Duke University Hospital Durham, North Carolina
ECU Health Medical Center Greenville, North Carolina
Eastern Maine Medical Center Bangor, Maine
Eden Medical Center, Castro Valley Castro Valley, California
Emory University Hospital Atlanta, Georgia
Erlanger Health System Chattanooga, Tennessee
Evanston Hospital Evanston, Illinois
Forsyth Medical Center Winston-Salem, North Carolina
Fort Sanders Regional Medical Center Knoxville, Tennessee
Froedtert Hospital Milwaukee, Wisconsin
Geisinger Medical Center Danville, Pennsylvania
George Washington University Hospital Washington D.C., District of Columbia
Good Samaritan Hospital West Islip, New York
Grady Memorial Hospital Delaware, Ohio
Greenville Hospital System Greenville, South Carolina
Hackensack University Medical Center Hackensack, New Jersey
Harborview Medical Center Seattle, Washington
Hartford Hospital Hartford, Connecticut
HealthPartners Methodist Hospital Saint Louis Park, Minnesota
Henry Ford Hospital Detroit, Michigan
Hoag Hospital Newport Beach Newport Beach, California
Hospital of the University of Pennsylvania Philadelphia, Pennsylvania
Houston Methodist Hospital Houston, Texas
Huntington Memorial Hospital Pasadena, California
IU Health Methodist Hospital Indianapolis, Indiana
Inova Fairfax Hospital Falls Church, Virginia
Jackson Memorial Hospital Miami, Florida
Javon Bea Hospital - Riverside Rockford, Illinois
Jefferson Abington Hospital Abington, Pennsylvania
Kaiser Permanente Fontana Medical Center Fontana, California
Kaiser Permanente Los Angeles Medical Center Los Angeles, California
Kaiser Permanente Redwood City Medical Center, Redwood City, CA Redwood City, California
Kaiser Permanente Sacramento Medical Center Sacramento, California
Kings County Hospital Center Brooklyn, New York
Lahey Hospital & Medical Center Burlington, Massachusetts
Lehigh Valley Hospital - Cedar Crest Allentown, Pennsylvania
Long Beach Memorial Medical Center Long Beach, California
Los Alamitos Medical Center Los Alamitos, California
Loyola University Medical Center Maywood, Illinois
M Health Fairview University of Minnesota Medical Center Minneapolis, Minnesota
Maimonides Medical Center Brooklyn, New York
Maine Medical Center Portland, Maine
Massachusetts General Hospital Boston, Massachusetts
Mayo Clinic Rochester, Minnesota
McLaren Flint Flint, Michigan
McLaren Macomb Mount Clemens, Michigan
MedStar Georgetown University Hospital Washington D.C., District of Columbia
Medical University of South Carolina University Hospital Charleston, South Carolina
Medstar Washington Hospital Center Washington D.C., District of Columbia
Memorial Hermann Texas Medical Center Houston, Texas
Mercy Hospital Oklahoma City Oklahoma City, Oklahoma
Mercy Hospital South St Louis, Missouri
Mercy Hospital Springfield Springfield, Missouri
Mercy Hospital St. Louis St Louis, Missouri
Mercy San Juan Medical Center Carmichael, California
Methodist University Hospital Memphis, Tennessee
Metro Health Hospital Wyoming, Michigan
MetroHealth Medical Center Cleveland, Ohio
Montefiore Medical Center The Bronx, New York
Morton Plant Hospital Clearwater, Florida
Moses H. Cone Memorial Hospital Greensboro, North Carolina
Mount Sinai West New York, New York
Munson Medical Center Traverse City, Michigan
NCH Hospital, Arlington Heights Arlington Heights, Illinois
NYC Health + Hospitals/Elmhurst Elmhurst, New York
NYP Columbia University Medical Center New York, New York
NYP Weill Cornell Medical Center New York, New York
NYU Langone Hospital - Brooklyn Brooklyn, New York
New Hanover Regional Medical Center Wilmington, North Carolina
New Hanover Regional Medical Center Wilmington, North Carolina
NewYork-Presbyterian Brooklyn Methodist Hospital Brooklyn, New York
North Shore University Hospital Manhasset, New York
OSF St. Francis Medical Center Peoria, Illinois
OSU Wexner Medical Center Columbus, Ohio
OU Medical Center Oklahoma City, Oklahoma
Ochsner Medical Center - Main Campus New Orleans, Louisiana
Oregon Health & Science University Hospital Portland, Oregon
Overlook Medical Center Summit, New Jersey
PIH Health Hospital - Whittier Whittier, California
PeaceHealth Sacred Heart Medical Center - RiverBend Springfield, Oregon
Penn State Hershey Medical Center Hershey, Pennsylvania
Presbyterian Medical Center Philadelphia, Pennsylvania
Providence St. Vincent Medical Center Portland, Oregon
Rancho Los Amigos National Rehabilitation Center Downey, California
Regions Hospital Saint Paul, Minnesota
Rhode Island Hospital Providence, Rhode Island
Riverside Methodist Hospital Columbus, Ohio
Ronald Reagan UCLA Medical Center Los Angeles, California
Rush University Medical Center Chicago, Illinois
SUNY Upstate Medical University Syracuse, New York
Saint Alphonsus Regional Medical Center - Boise Boise, Idaho
San Francisco General Hospital San Francisco, California
Santa Barbara Cottage Hospital Santa Barbara, California
Semmes Murphey Main Campus Memphis, Tennessee
St. Cloud Hospital Saint Cloud, Minnesota
St. David's Medical Center Austin, Texas
St. John Medical Center Tulsa, Oklahoma
St. John's Hospital Springfield, Illinois
St. Joseph's Hospital Tucson, Arizona
St. Joseph's Hospital and Medical Center Phoenix, Arizona
St. Jude Medical Center Fullerton, California
St. Mary's Medical Center Grand Junction, Colorado
Stanford University Medical Center Palo Alto, California
Staten Island University Hospital - North Campus Staten Island, New York
Stony Brook University Hospital Stony Brook, New York
Strong Memorial Hospital Rochester, New York
Swedish Medical Center - Cherry Hill Campus Seattle, Washington
Tampa General Hospital Tampa, Florida
Temple University Hospital Philadelphia, Pennsylvania
The Mount Sinai Hospital New York, New York
The Queen's Medical Center Honolulu, Hawaii
The University of Vermont Medical Center Burlington, Vermont
Thomas Jefferson University Hospital Philadelphia, Pennsylvania
Trinity Health Saint Mary's Grand Rapids, Michigan
Trinity Health Saint Mary's Grand Rapids, Michigan
Tufts Medical Center Boston, Massachusetts
UAMS Medical Center Little Rock, Arkansas
UC Davis Medical Center Sacramento, California
UC Irvine Medical Center Orange, California
UF Health Jacksonville Jacksonville, Florida
UH Cleveland Medical Center Cleveland, Ohio
UMass Memorial Medical Center Worcester, Massachusetts
UPMC Presbyterian Hospital Pittsburgh, Pennsylvania
UT Southwestern Medical Center Dallas, Texas
UVA Medical Center Charlottesville, Virginia
United Hospital, St. Paul Saint Paul, Minnesota
University of Alabama Hospital Birmingham, Alabama
University of Chicago Medical Center Chicago, Illinois
University of Cincinnati Medical Center Cincinnati, Ohio
University of Colorado Hospital Aurora, Colorado
University of Illinois Hospital Chicago, Illinois
University of Iowa Medical Center Iowa City, Iowa
University of Kansas Hospital Kansas City, Kansas
University of Kentucky Hospital Lexington, Kentucky
University of Louisville Hospital Louisville, Kentucky
University of Michigan University Hospital Ann Arbor, Michigan
University of Mississippi Medical Center Jackson, Mississippi
University of Missouri Health Care Columbia, Missouri
University of Nebraska Medical Center Omaha, Nebraska
University of New Mexico Hospital Albuquerque, New Mexico
University of North Carolina Medical Center Chapel Hill, North Carolina
University of South Alabama University Hospital Mobile, Alabama
University of Texas Health Science Center San Antonio San Antonio, Texas
University of Utah Healthcare Salt Lake City, Utah
VCU Medical Center Richmond, Virginia
Vanderbilt University Hospital Nashville, Tennessee
Vassar Brothers Medical Center Poughkeepsie, New York
Virginia Mason Medical Center Seattle, Washington
WVU Healthcare Ruby Memorial Hospital Morgantown, West Virginia
Wake Forest Baptist Medical Center Winston-Salem, North Carolina
Wellstar Kennestone Hospital Marietta, Georgia
Westchester Medical Center Valhalla, New York
Yale New Haven Hospital New Haven, Connecticut

A Trial of Robotic Versus Open Hysterectomy Surgery in Cervix Cancer (ROCC)

Jennifer Klein, MEd - jklein@gog.org

NCT04831580
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Inclusion Criteria:

• Patient must have histologically confirmed adenocarcinoma (usual/classic/NOS), squamous cell carcinoma, adenosquamous carcinoma (Including glassy cell)
• Patient must be FIGO Stage IA2, IBI, IB2 (2018 staging) without evidence of definitive parametrial, vaginal, nodal or distant metastases on exam or imaging. Patients with tumor size less than or equal to 4 cm confirmed on MRI prior to randomization are eligible.
• Patient must have uterine size \<12 cm AND felt to be appropriate for vaginal delivery of the specimen per investigator.
• Patient must be suitable surgical candidate with preoperative assessments such as labs and EKG performed per institutional standard and agree to be randomized to undergo open or robotic radical (or simple) hysterectomy. NOTE: Simple hysterectomy will be allowed in patients who meet the following criteria:
• pelvic MRI must demonstrate a maximal tumor size of 2 cm or less AND
• less than 50% stromal invasion on MRI if tumor present or less than 10 mm of stromal invasion if an excisional (cold knife or LEEP) has been performed. Submission of source documents in the GOG Partners Source Document Portal will be required prior to randomization for review and confirmation of simple hysterectomy being met (see Section 6.0 for instructions).
• Patient must be age 18 years or older.
• Patient must have ECOG performance status 0-1.
• Patient must have a negative urine pregnancy test within 30 days of surgery in pre-menopausal women.
• Patient must have signed an approved informed consent and authorization permitting the release of personal health information.
Exclusion Criteria:

• Patients with any tumor histology other than those listed above, specifically excluding the following histologies: neuroendocrine, other adenocarcinoma (gastric type, endometrioid, clear cell, serous, signet ring, minimal deviation)
• Patients with FIGO stage 1A1, IB3, II-IV (2018 staging).
• Patient with inability to receive an MRI.
• Patients with a tumor size greater than 4cm or on MRI confirmed prior to randomization are excluded. Patients with definite evidence of vaginal/parametrial involvement on MRI are excluded; if MRI findings are not definitive, then clinical examination must also not reveal parametrial or vaginal extension).
• Patients with evidence of metastatic disease (imaging or histologically positive lymph nodes).
• Patients with a history of prior pelvic or abdominal radiotherapy.
• Patients with a prior malignancy \< 5 years from enrollment with the exception of non-melanoma skin cancer.
• Patients who are unable to withstand prolonged lithotomy or steep trendelenberg.
• Patient compliance and geographic proximity that do not allow adequate follow-up.
• Patients with poorly controlled HIV with CD4 counts \<500.
DEVICE: da Vinci, OTHER: open surgery
Cervical Cancer
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Show 136 locations

Study Locations

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Location Contacts
AHN West Penn Hospital Pittsburgh, Pennsylvania - (janke.mainsmason@ahn.org)
Abington Memorial Hospital Abington, Pennsylvania Ashley Douglas - (ashley.douglas@jefferson.edu)
Ascension Medical Group St. Vincent's Obstetrics and Gynecology Jacksonville, Florida Nicole Antenucci - (nicole.antenucci@ascension.org)
Asplundh Cancer Pavillion Willow Grove, Pennsylvania Ashley Douglas - (ashley.douglas@jefferson.edu)
Baptist Health Miami, Florida Lauren Higgins - (lauren.higgins@bhsi.com)
Baptist Health Lexington Lexington, Kentucky Lauren Higgins - (lauren.higgins@bhsi.com)
Baystate Medical Center Springfield, Massachusetts
California Pacific Medical Center-Research Institute San Francisco, California Claudia Chavez - (chavezck@sutterhealth.org)
Center of Hope Reno, Nevada Shannon White Pierpoint - (spierpoint@cohreno.com)
Centre Hospitalier de l'Université de Montréal Montreal, Quebec Mathilde Duplaix - (mathilde.duplaix.chum@ssss.gouv.qc.ca)
Chattanooga's Program in Women's Oncology Chattanooga, Tennessee Kimberly Donelson - (Kimberly.Donelson@erlanger.org)
City of Hope Duarte, California Raechelle Tinsley - (RTinsley@coh.org)
City of Hope - Upland Upland, California Raechelle Tinsley - (rtinsley@coh.org)
City of Hope Orange County Lennar Foundation Cancer Irvine, California Raechelle Tinsley - (rtinsley@coh.org)
David C. Pratt Center St. Louis, Missouri Crystal Tindall - (crystal.tindall@mercy.net)
Duke Cancer Center Durham, North Carolina Taylor Hayes - (taylor.hayes@duke.edu)
Duke Cancer Center Durham, North Carolina Lauren March - (lauren.march@duke.edu)
Duke University Hospital Durham, North Carolina Taylor Hayes - (taylor.hayes@duke.edu)
FirstHealth Outpatient Cancer Center Pinehurst, North Carolina Tina Thompson - (tpthompson@firsthealth.org)
Georgian Cancer Center at Augusta University Augusta, Georgia Angela Goebel - (agoebel@augusta.edu)
Harford HealthCare Cancer Institute at the Hospital of Central Connecticut New Britain, Connecticut Siobhan Reilly - (mailto:siobhan.reilly@hhchealth.org)
Hartford Healthcare Cancer Institute at Hartford Hospital Hartford, Connecticut Siobhan Reilly - (mailto:siobhan.reilly@hhchealth.org)
Hartford Healthcare Medical Group-Manchester Manchester, Connecticut Siobhan Reilly - (mailto:siobhan.reilly@hhchealth.org)
Hartford Hospital Hartford, Connecticut Siobhan Reilly - (mailto:siobhan.reilly@hhchealth.org)
Hoag Gynecologic Oncology Newport Beach, California Ana Navarrete - (ana.navarrete@hoag.org)
Hoag Memorial Hospital Presbyterian Newport Beach, California Ana Navarrete - (ana.navarrete@hoag.org)
James Cancer Hospital & Solove Research Institute at The Ohio State University Comprehensive Cancer Center Columbus, Ohio Callan Myercough - (callan.myerscough@osumc.edu)
JamesCare Gynecologic Oncology at Mill Run Hilliard, Ohio Callan Myerscough - (macallan.myerscough@osumc.edu)
Josie Robertson Surgery Center New York, New York Josie Anderson - (andersj@mskcc.org)
Kettering Health Cancer Center Kettering, Ohio Julie Carstens - (julie.carstens@ketteringhealth.org)
LSU Health New Orleans New Orleans, Louisiana Dina Brackman - (dbrack@lsuhsc.edu)
Laura and Issac Perlmutter Cancer Center at NYU Langone New York, New York Kathryn Allen - (mailto:Kathryn.Allen@nyulangone.org)
Laura and Issac Perlmutter Cancer Center at NYU Langone New York, New York Kathryn Allen - (mailto:Kathryn.Allen@nyulangone.org)
Laura and Issac Perlmutter Cancer Center at NYU Langone-East 34th Street New York, New York Kathryn Allen - (mailto:Kathryn.Allen@nyulangone.org)
Legacy Good Samaritan Medical Center-Gynecological Oncology Group Portland, Oregon
Legacy Meridian Park Medical Center-Legacy Medical Gynecologic Oncology Tualatin, Oregon
Legacy Salmon Creek Medical Center-Legacy Medical Group Gynecologic Oncology Vancouver, Washington Lauren Elliot - (lelliott@lhs.org)
M Health Fairview University of Minnesota Medical Center-East Bank Hospital Minneapolis, Minnesota Erin Zielinksi - (eezielin@umn.edu)
M Health Fairview University of Minnesota Medical Center-East Bank Hospital Minneapolis, Minnesota Erin Zielinksi - (eezielin@umn.edu)
Magee - Womens Hospital of UPMC Pittsburgh, Pennsylvania Jessica Yauch - (yauchj@upmc.edu)
Maine Medical Partners-Woman's Health-Division of Gynecologic Oncology Scarborough, Maine Robin Donovan - (donovr@mmc.org)
McGill University Health Centre-Glen Site Montréal, Quebec Phuong-Nam Nguyen - (mailto:phuong-nam.nguyen@mail.mcgill.ca)
Memorial Sloan Kettering (Basking Ridge) Basking Ridge, New Jersey Josie Anderson - (andersj@mskcc.org)
Memorial Sloan Kettering (Bergen) Montvale, New Jersey Josie Anderson - (andersj@mskcc.org)
Memorial Sloan Kettering (Commack) Commack, New York Josie Anderson - (andersj@mskcc.org)
Memorial Sloan Kettering (Monmouth) Middletown, New York Josie Anderson - (andersj@mskcc.org)
Memorial Sloan Kettering (Nassau) Uniondale, New York Josie Anderson - (andersj@mskcc.org)
Memorial Sloan Kettering (Westchester) Harrison, New York Josie Anderson - (andersj@mskcc.org)
Memorial Sloan Kettering Cancer Center (Main Campus) New York, New York Josie Anderson - (mailto:andersj@mskcc.org)
Mercy Hospital Coon Rapids, Minnesota Jennifer Mosley - (Jennifer.mosley@hcahealthcare.com)
Mercy Hospital Coon Rapids, Minnesota Jennifer Mosley - (Jennifer.mosley@hcahealthcare.com)
Miami Cancer Institute at Baptist Health, Inc. Miami, Florida Jacqueline Lebron - (jacquelile@baptisthealth.net)
Miami Cancer Institute at Baptist Health, Inc. Miami, Florida Stephany Fuentes Angulo - (Stephany.FuentesAngulo@baptisthealth.net)
Minnesota Oncology Hematology Minneapolis, Minnesota Jessica Thomes-Pepin - (jessica.thomespepin@usoncology.com)
Mount Sinai Comprehensive Cancer Center Miami Beach, Florida
NHPP/Gynecologic Oncology at New Hyde Park New Hyde Park, New York Batool Mubashar - (mailto:bmubashar@northwell.edu)
NYU Langone Ambulatory Care Bay Ridge Brooklyn, New York Kathryn Allen - (mailto:Kathryn.Allen@nyulangone.org)
NYU Langone Hospital-Brooklym Brooklyn, New York Kathryn Allen - (mailto:Kathryn.Allen@nyulangone.org)
NYU Langone Medical Center (Tisch Hospital) New York, New York Kathryn Allen - (mailto:Kathryn.Allen@nyulangone.org)
Northwell Health Physician Partners/Gynecological Oncology at Brightwaters Brightwaters, New York Batool Mubashar - (mailto:bmubashar@northwell.edu)
Northwell Health/Huntington Hospital Huntington, New York Batool Mubashar - (mailto:bmubashar@northwell.edu)
Northwell Health/Long Island Jewish Medical Center New Hyde Park, New York Batool Mubashar - (mailto:bmubashar@northwell.edu)
Northwell Health/South Shore University Hospital Bay Shore, New York Batool Mubashar - (mailto:bmubashar@northwell.edu)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
Novant Health Cancer Institute Charlotte, North Carolina - (kashah@novanthealth.org)
OSU Wexner Medical Center Hospital East Columbus, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Martha Morehouse Outpatient Care Columbus, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Outpatient Care Dublin Dublin, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Outpatient Care East Columbus, Ohio Callan Myserscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Outpatient Care Gahanna Columbus, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Outpatient Care Lewis Center Lewis Center, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Outpatient Care New Albany Westerville, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Outpatient Care Upper Arlington Columbus, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center Stefanie Spielman Comprehensive Breast Center Columbus, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
OSU Wexner Medical Center University Hospital Columbus, Ohio Callan Myerscough - (callan.myerscough@osumc.edu)
Orlando Health Cancer Center Orlando, Florida
Orlando Health Winnie Palmer Hospital for Woman and Babies Orlando, Florida Jennifer Durand - (Jennifer.durand@orlandohealth.com)
Palo Alto Medical Foundation Palo Alto, California Claudia Chavez - (chavezck@sutterhealth.org)
Providence Center Institute Franz Clinic Portland, Oregon Nora Auston - (Nora.Auston@providence.org)
South Miami Hospital Miami, Florida Jacqueline Lebron - (jacquelile@baptisthealth.net)
South Miami Hospital Miami, Florida Stephany Fuentes Angulo - (Stephany.FuentesAngulo@baptisthealth.net)
Southeastern Regional Medical Center LLC Newnan, Georgia Nikki Morris - (mailto:nikki.morris@ctca-hope.com)
St. Elizabeth Healthcare Edgewood, Kentucky Becky Dixon - (becky.dixon@stelizabeth.com)
St. Vincent Hospital and Health Care Center Inc Indianapolis, Indiana
St. Vincent Hospital and Health Care Center, Inc Indianapolis, Indiana
Stanford Hospital Stanford, California Samya Konda - (skonda@stanford.edu)
Stephenson Cancer Center Oklahoma City, Oklahoma Morgan Hays - (mailto:morgan-hays@ouhsc.edu)
Summa Health Jean and Milton Copper Pavilion Akron, Ohio Danielle McCutcheon - (mccutcheond@summahealth.org)
Summa Health Jean and Milton Copper Pavillion Akron, Ohio Danielle McCutcheon - (mamccutcheond@summahealth.org)
Tampa General Hospital Tampa, Florida
Texas Oncology Dallas, Texas Nori Sullivan - (mailto:nori.sullivan@usoncology.com)
Texas Oncology- Baylor Charles A. Sammons Cancer Center Dallas, Texas Christine Terraciano - (christine.terraciano@usoncology.com)
Texas Oncology- GYN ONC DFWW Bedford, Texas Nori Sullivan - (mailto:nori.sullivan@usoncology.com)
Texas Oncology-Austin Austin, Texas Kelli Watkins - (kelli.watkins@mckesson.com)
Texas Oncology-DFWW Bedford, Texas Sarah Wade - (mailto:Sarah.Wade@usoncology.com)
Texas Oncology-GYN ONC DFWW Fort Worth, Texas Nori Sullivan - (mailto:nori.sullivan@usoncology.com)
Texas Oncology-San Antonio San Antonio, Texas Riquanda Walker - (Riquanda.Walker@McKesson.com)
Texas Oncology-The Woodlands, Gynecologic Oncology The Woodlands, Texas Kelli Watkins - (Kelli.Watkins@mckesson.com)
The Blavatnik Family - Chelsea Medical Center at Mount Sinai New York, New York Neha Kumarley - (Kuneha.kumarley@mssm.edu)
The West Clinic, PLLC dba West Cancer Center Germantown, Tennessee Joslyn Walker - (jowalker@westclinic.com)
TriHealth Cancer Institute-Good Samaritan Hospital Cincinnati, Ohio Diann Fischesser - (mailto:diann_fischesser@trihealth.com)
TriHealth Cancer Institute-Thomas Comprehensive Care Center Cincinnati, Ohio Diann Fischesser - (mailto:diann_fischesser@trihealth.com)
University of California San Diego Medical Center La Jolla, California - (aocronin@health.ucsd.edu)
University of California San Diego Medical Center La Jolla, California - (aocronin@health.ucsd.edu)
University of California San Diego Medical Center La Jolla, California - (aocronin@health.ucsd.edu)
University of California San Diego Medical Center La Jolla, California - (aocronin@health.ucsd.edu)
University of California San Diego Moores Cancer Center La Jolla, California - (aocronin@health.ucsd.edu)
University of Cleveland Medical Center Cleveland, Ohio Lauren Patrick - (Lauren.Patrick@uhhospitals.org)
University of New Mexico Comprehensive Cancer Center Albuquerque, New Mexico Rebecca Baca - (rebaca@salud.unm.edu)
University of Pennsylvania Health System, Perelman Center for Advanced Medicine Philadelphia, Pennsylvania Christine Yang - (christine.yang@pennmedicine.upenn.edu)
University of Texas Southwestern Medical Center Dallas, Texas Annette Paulsen - (mailto:Annette.Paulsen@UTSouthwestern.edu)
University of Texas Southwestern Medical Center-Simmons Cancer Center Dallas, Texas Annette Paulsen - (mailto:Annette.Paulsen@UTSouthwestern.edu)
University of Texas Southwestern Medical Center-WIlliam P. Clements Jr. University Hospital Dallas, Texas Annette Paulsen - (Annette.Paulsen@UTSouthwestern.edu)
University of Texas Southwestern Medical Center-Zale Lipshy University Hospital Dallas, Texas Annette Paulsen - (Annette.Paulsen@UTSouthwestern.edu)
University of Virginia Charlottesville, Virginia Rachel Lacy - (rmc9p@hscmail.mcc.virginia.edu)
University of Virginia Comprehensive Cancer Center Charlottesville, Virginia Rachel Lacy - (mrmc9p@hscmail.mcc.virginia.edu)
University of Wisconsin Clinical Science Center Madison, Wisconsin Claire Kostechka - (kostechka@wisc.edu)
VCU Health Emergency Center at New Kent Quinton, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
VCU Health Short Pump Pavillion Richmond, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
VCU Health at GreenGate Henrico, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
VCU Health at Tappahannock Hospital Tappahannock, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
VCU Health-William and Mary Williamsburg, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
VCU Massey Cancer Center at Stony Point Richmond, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
Virginia Commonwealth University Massey Cancer Center Richmond, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
Virginia Commonwealth University-Main Hospital Richmond, Virginia Sonya Washington - (mailto:slwashington@vcu.edu)
West Virginia Morgantown, West Virginia Christina Martinelli - (mailto:christina.martinelli@hsc.wvu.edu)
West Virginia University Morgantown, West Virginia Christina Martinelli - (mailto:christina.martinelli@hsc.wvu.edu)
Western Regional Medical Center LLC Goodyear, Arizona Nikki Morris - (mailto:nikki.morris@ctca-hope.com)
Willis-Knighton Physician Network Gynecologic Oncology Associates Shreveport, Louisiana Carrie Key, RN - (ckay@wkhs.com)
Women's and Infants Hospital of Rhode Island Program in Women's Oncology Providence, Rhode Island Ann John - (ajohn@wihri.org)

A Study of Nivolumab-relatlimab Fixed-dose Combination Versus Regorafenib or TAS-102 in Participants With Later-lines of Metastatic Colorectal Cancer (RELATIVITY-123)

BMS Study Connect Contact Center www.BMSStudyConnect.com - Clinical.Trials@bms.com

NCT05328908
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Inclusion Criteria:

• Histological confirmed previously treated colorectal cancer with adenocarcinoma histology with metastatic or recurrent unresectable disease at study entry
• Participants must have:
• progressed during or within approximately 3 months following the last administration of approved standard therapies (at least 1, but not more than 4 prior lines of therapies), which must include a fluoropyrimidine, oxaliplatin, irinotecan, an anti-VEGF therapy, and anti-EGFR therapy (if KRAS wild-type), if available in the respective country, or;
• been intolerant to prior systemic chemotherapy regimens if there is documented evidence of clinically significant intolerance despite adequate supportive measures
• Must have sufficient tumor tissue & evaluable PD-L1 expression to meet the study requirements
• Must have measurable disease per RECIST v1.1. Participants with lesions in a previously irradiated field as the sole site of measurable disease will be permitted to enroll provided the lesion(s) have demonstrated clear progression and can be measured accurately
Exclusion Criteria:

• Prior treatment with either an immunotherapy or with regorafenib or with TAS-102
• Untreated central nervous system (CNS) metastases, participants are eligible if CNS metastases have been treated and participants have neurologically returned to baseline (except for residual signs or symptoms related to the CNS treatment)
• History of refractory hypertension not controlled with anti-hypertensive therapy, myocarditis (regardless of etiology), uncontrolled arrhythmias, acute coronary syndrome within 6 months prior to dosing, Class II congestive heart failure (as per the New York Heart Association Functional Classification), interstitial lung disease/pneumonitis or an active, known or suspected autoimmune disease
• Confirmed tumor microsatellite instable high/deficient mismatch repair (MSI-H/dMMR) status as per local standard testing; MSI/MMR test results from initial diagnosis are acceptable. Other protocol-defined inclusion/exclusion criteria apply
Drug: Nivolumab-relatlimab FDC, Drug: Regorafenib, Drug: TAS-102
Colorectal Neoplasms
Micro-satellite Stable (MSS) Metastatic Colorectal Cancer (mCRC), Relatlimab, Nivolumab, BMS-986213, Regorafenib, Stivarga, Lonsurf
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Study Locations

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Location Contacts
Astera Cancer Care East Brunswick, New Jersey Phillip Reid, Site 0043
Baptist Hospital of Miami Miami, Florida Antonio Ucar, Site 0025
Charleston Hematology Oncology Associates (CHOA) Charleston, South Carolina David Ellison, Site 0008
City of Hope Duarte, California
Duke University Medical Center Durham, North Carolina Michael Morse, Site 0009
Eastern Connecticut Hematology and Oncology (ECHO) Norwich, Connecticut Dennis Slater, Site 0117
Fort Wayne Medical Oncology and Hematology Fort Wayne, Indiana Sunil Babu, Site 0081
Fox Chase Cancer Center Philadelphia, Pennsylvania Namrata Vijayvergia, Site 0147
Good Samaritan Hospital West Islip, New York David Draper, Site 0082
Highlands Oncology Group - Springdale Springdale, Arkansas J.Thaddeus Beck, Site 0044
Local Institution - 0001 Lenexa, Kansas Site 0001
Local Institution - 0002 London,
Local Institution - 0003 Oakland, California Site 0003
Local Institution - 0004 ABB, Buenos Aires F.D. Site 0004
Local Institution - 0007 Santiago, Santiago Metropolitan Site 0007
Local Institution - 0010 Lille, Hauts-de-France Site 0010
Local Institution - 0014 Strasbourg, Alsace Site 0014
Local Institution - 0015 Paris, Site 0015
Local Institution - 0016 Lima, LIM Site 0016
Local Institution - 0017 Toulouse, Haute-Garonne Site 0017
Local Institution - 0018 La Tronche, Isère Site 0018
Local Institution - 0019 Villejuif, Val-de-Marne Site 0019
Local Institution - 0020 Badalona, Barcelona Site 0020
Local Institution - 0021 La Jolla, California Site 0021
Local Institution - 0022 Yvoir, Namur
Local Institution - 0023 Ghent, Oost-Vlaanderen Site 0023
Local Institution - 0024 Sint-Niklaas, Oost-Vlaanderen Site 0024
Local Institution - 0026 New York, New York Site 0026
Local Institution - 0027 New Orleans, Louisiana Site 0027
Local Institution - 0028 Ravenna, Emilia-Romagna Site 0028
Local Institution - 0029 Parma, Site 0029
Local Institution - 0030 Beijing, Beijing Municipality Site 0030
Local Institution - 0033 Wenzhou, Zhejiang Site 0033
Local Institution - 0034 Naples, Site 0034
Local Institution - 0035 New York, New York Site 0035
Local Institution - 0036 Aviano, Friuli Venezia Giulia Site 0036
Local Institution - 0037 Portland, Oregon Site 0037
Local Institution - 0038 Portland, Oregon Site 0038
Local Institution - 0039 Zuerich, Site 0039
Local Institution - 0040 Evanston, Illinois Site 0040
Local Institution - 0041 St.Gallen, HE Site 0041
Local Institution - 0045 Seoul, Seoul-teukbyeolsi [Seoul] Site 0045
Local Institution - 0046 Suwon, Kyǒnggi-do Site 0046
Local Institution - 0050 Grand Rapids, Michigan Site 0050
Local Institution - 0051 Sevilla, MZ Site 0051
Local Institution - 0052 Mainz, Rheinland-Pfalz Site 0052
Local Institution - 0053 Burlington, Ontario Site 0053
Local Institution - 0054 Athens, Attikí Site 0054
Local Institution - 0055 Lima, Site 0055
Local Institution - 0056 Thessaloniki, Kentrikí Makedonía Site 0056
Local Institution - 0057 Hannover, Site 0057
Local Institution - 0058 Chicago, Illinois Site 0058
Local Institution - 0059 Los Angeles, California Site 0059
Local Institution - 0060 Chaïdári, Attikí Site 0060
Local Institution - 0061 London, Kensington and Chelsea Site 0061
Local Institution - 0062 Thessaloniki, Thessaloníki Site 0062
Local Institution - 0063 Brno, JM
Local Institution - 0064 Praha 5, Prague Site 0064
Local Institution - 0066 Massillon, Ohio Site 0066
Local Institution - 0067 Hackensack, New Jersey Site 0067
Local Institution - 0068 Seoul, Seoul-teukbyeolsi [Seoul] Site 0068
Local Institution - 0069 Bengaluru, Karnataka Site 0069
Local Institution - 0070 New Delhi, National Capital Territory of Delhi Site 0070
Local Institution - 0072 Gurugram, Haryana Site 0072
Local Institution - 0073 Ahmedabad, Gujarat Site 0073
Local Institution - 0074 Montpellier, Languedoc-Roussillon Site 0074
Local Institution - 0075 Chengdu, Sichuan Site 0075
Local Institution - 0076 Villejuif, Val-de-Marne Site 0076
Local Institution - 0077 Mumbai, Maharashtra Site 0077
Local Institution - 0078 Howrah, West Bengal Site 0078
Local Institution - 0080 Iowa City, Iowa Site 0080
Local Institution - 0083 Ahmedabad, Gujarat Site 0083
Local Institution - 0084 Strasbourg, Alsace Site 0084
Local Institution - 0085 Gainesville, Florida Site 0085
Local Institution - 0086 Linz, Site 0086
Local Institution - 0087 Richmond, Virginia Site 0087
Local Institution - 0088 Pittsburgh, Pennsylvania Site 0088
Local Institution - 0089 Cheongju-si, Chungcheongbuk-do [Chungbuk] Site 0089
Local Institution - 0090 Bordeaux, Aquitaine Site 0090
Local Institution - 0091 Victoria, British Columbia Site 0091
Local Institution - 0092 Seoul, Seoul-teukbyeolsi [Seoul] Site 0092
Local Institution - 0093 Salamanca, Site 0093
Local Institution - 0094 Córdoba, Córdoba Province Site 0094
Local Institution - 0098 Fort Collins, Colorado Site 0098
Local Institution - 0099 Sherbrooke, Quebec Site 0099
Local Institution - 0100 Seoul, Seoul-teukbyeolsi [Seoul] Site 0100
Local Institution - 0101 Erlangen, Bavaria Site 0101
Local Institution - 0102 Québec, Quebec Site 0102
Local Institution - 0103 Drammen, Buskerud Site 0103
Local Institution - 0104 Atlanta, Georgia Site 0104
Local Institution - 0105 Oslo, Site 0105
Local Institution - 0106 Bergen, Hordaland Site 0106
Local Institution - 0107 Wichita, Kansas Site 0107
Local Institution - 0108 Wuhan, Hubei Site 0108
Local Institution - 0109 Hefei, Anhui Site 0109
Local Institution - 0110 Glasgow, Glasgow City Site 0110
Local Institution - 0111 Qingdao, Shandong Site 0111
Local Institution - 0112 Toronto, Ontario Site 0112
Local Institution - 0113 Charlottesville, Virginia Site 0113
Local Institution - 0114 Busan, Pusan-Kwangyǒkshi Site 0114
Local Institution - 0115 Bucharest, Site 0115
Local Institution - 0116 Deagu, Taegu-Kwangyǒkshi Site 0116
Local Institution - 0118 Sendai, Miyagi Site 0118
Local Institution - 0119 Iași, Site 0119
Local Institution - 0120 Bucharest, Bucharest Site 0120
Local Institution - 0121 Shimotsuga, Tochigi Site 0121
Local Institution - 0122 Osaka, Site 0122
Local Institution - 0123 Bucharest, Bucharest Site 0123
Local Institution - 0124 Iași, Site 0124
Local Institution - 0125 Ōsaka-sayama, Osaka
Local Institution - 0126 Amagasaki, Hyōgo Site 0126
Local Institution - 0128 Mexico City, Mexico City Site 0128
Local Institution - 0129 Bogotá, Distrito Capital De Bogotá Site 0129
Local Institution - 0131 Busan, Pusan-Kwangyǒkshi Site 0131
Local Institution - 0133 Cluj-Napoca,
Local Institution - 0134 Chongqing, Chongqing Site 0134
Local Institution - 0135 Stockholm, Site 0135
Local Institution - 0136 Buenos Aires,
Local Institution - 0138 Bogota, Site 0138
Local Institution - 0139 Monterrey, Nuevo León Site 0139
Local Institution - 0141 Aguascalientes, AGU Site 0141
Local Institution - 0142 Pembroke Pines, Florida Site 0142
Local Institution - 0143 Columbus, Georgia Site 0143
Local Institution - 0144 San Miguel, LIM Site 0144
Local Institution - 0146 Huaian, Jiangsu Site 0146
Local Institution - 0148 Katowice, Site 0148
Local Institution - 0149 Goyang-si, Kyǒnggi-do Site 0149
Local Institution - 0150 Bursa, Site 0150
Local Institution - 0151 Guangzhou, Guangdong Site 0151
Local Institution - 0152 Xian, SN Site 0152
Local Institution - 0153 Chicago, Illinois Site 0153
Local Institution - 0155 Ürümqi, Xinjiang Site 0155
Local Institution - 0156 Piura, PIU Site 0156
Local Institution - 0157 Valencia, Comunidad Valencia Site 0157
Local Institution - 0158 New York, New York Site 0158
Local Institution - 0159 Chengdu Shi, Site 0159
Local Institution - 0160 Budapest, Pest Site 0160
Local Institution - 0161 Auderghem, Bruxelles-Capitale, Région de Site 0161
Local Institution - 0162 Bron, Rhône Site 0162
Local Institution - 0163 Harderwijk, Gelderland
Massachusetts General Hospital, Boston, Massachusetts Aparna Parikh, Site 0140
Mayo Clinic in Arizona - Phoenix Phoenix, Arizona
Northside Hospital - Atlanta Atlanta, Georgia Ioana Bonta, Site 0031
Perelman School of Medicine at the University of Pennsylvania Philadelphia, Pennsylvania
Rush University Medical Center Chicago, Illinois
Sanford Research Sioux Falls, South Dakota Jonathan Bleeker, Site 0096
St. Luke's Cancer Institute - Boise Boise, Idaho Dan Zuckerman, Site 0071
Tennessee Oncology Nashville, Tennessee Meredith Pelster, Site 0127
The Center for Cancer and Blood Disorders Fort Worth, Texas Henry Xiong, Site 0097
The James Cancer Hospital Columbus, Ohio Pannaga Malalur, Site 0095
The James Cancer Hospital and Solove Research Institute at The Ohio State University Comprehensive C Columbus, Ohio Anne Noonan, Site 0079
Thomas Jefferson University - Clinical Trials Office-Medical Oncology Philadelphia, Pennsylvania Atrayee Basu-Mallick, Site 0130
USC Norris Comprehensive Cancer Center Los Angeles, California Heinz-Josef Lenz, Site 0012
University of Michigan - Rogel Cancer Center Ann Arbor, Michigan John Krauss, Site 0042
University of Wisconsin-Madison - Wisconsin Institutes for Medical Research (WIMR) Madison, Wisconsin Dustin Deming, Site 0005
Virginia Commonwealth University Massey Cancer Center Richmond, Virginia Khalid Matin, Site 0132

A Study of BMS-986406 as Monotherapy and Combination Therapies in Participants With Advanced Tumors

BMS Study Connect Contact Center www.BMSStudyConnect.com - Clinical.Trials@bms.com

NCT05298592
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Inclusion Criteria:

• Histologically or cytologically confirmed locally advanced unresectable, metastatic, or recurrent malignant tumor. Eligible tumor types are non-small cell lung cancer (NSCLC), renal cell carcinoma (RCC), pancreatic ductal adenocarcinoma (PDAC), gastric/gastroesophageal junction, castration-resistant prostate cancer (CRPC), ovarian, squamous cell carcinoma of the head and neck (SCCHN), bladder, melanoma, mesothelioma, triple negative breast cancer (TNBC), and soft tissue sarcoma, except for participants with tumors with central nervous system (CNS) metastases as the only site of active disease
• Measurable disease by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST v1.1), Prostate Cancer Working Group 3 (PCWG3) (for prostate cancer), or modified Response Evaluation Criteria in Solid tumors (mRECIST) (for mesothelioma)
• Eastern Cooperative Oncology Group Performance Status of 0 or 1
• Adequate organ function
Exclusion Criteria:

• Prior organ or tissue allograft
• Leptomeningeal metastases
• Untreated CNS metastases
• Serious or uncontrolled medical disorders Other protocol-defined inclusion/exclusion criteria apply
Biological: BMS-986406, Biological: Nivolumab
Advanced Cancer
Opdivo®, Immunotherapy
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Study Locations

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Location Contacts
Carolina BioOncology Institute, PLLC Huntersville, North Carolina John Powderly, Site 0002
Fox Chase Cancer Center Philadelphia, Pennsylvania
Hackensack University Medical Center Hackensack, New Jersey Martin Gutierrez, Site 0001
Local Institution - 0007 Santiago, Santiago Metropolitan Site 0007
Local Institution - 0008 Ciudad Autónoma de Buenos Aires, Buenos Aires Site 0008
Local Institution - 0009 Pittsburgh, Pennsylvania Site 0009
Local Institution - 0011 Paris, Site 0011
Local Institution - 0012 Marseille, Site 0012
Local Institution - 0014 Strasbourg, Alsace Site 0014
Local Institution - 0015 Paris, Site 0015
Local Institution - 0016 Lima, LIM Site 0016
Local Institution - 0017 Toulouse, Haute-Garonne Site 0017
Local Institution - 0018 La Tronche, Isère Site 0018
Local Institution - 0022 Yvoir, Namur Site 0022
Local Institution - 0023 Ghent, Oost-Vlaanderen Site 0023
Local Institution - 0024 Sint-Niklaas, Oost-Vlaanderen Site 0024
Mary Crowley Cancer Research - Medical City Hospital Dallas, Texas Minal Barve, Site 0005
NYU Langone Medical Center New York, New York Kristen Spencer, Site 0019
Sanford Cancer Center Sioux Falls, South Dakota Steven Powell, Site 0013
The Angeles Clinic and Research Institute, A Cedars-Sinai Affiliate Los Angeles, California Omid Hamid, Site 0004
The Kirklin Clinic of UAB Hospital, Birmingham, AL Birmingham, Alabama Mehmet Akce, Site 0021
UCLA Health Los Angeles, California Zev Wainberg, Site 0020
VCU Massey Cancer Center Richmond, Virginia Andrew Poklepovic, Site 0006

Predicting Outcomes in Nonalcoholic Steatohepatitis With Advanced Fibrosis

Mohammad S Siddiqui, MD - mohammad.siddiqui@vcuhealth.org

NCT05720663
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Inclusion Criteria:
Adult patients with presence of NAFLD associated cirrhosis. * Cirrhosis: biopsy confirmed or Agile F (F4) score \> 0.45 * NAFLD as an etiology of liver disease will be determined based on presence of any of the following: * Biopsy showing \>5% steatosis or * CAP \> 280 dB/m or MR-PDFF\>5% * If CAP \< 280 dB/m or MR-PDFF \<5%, then must have type 2 diabetes and or 2 or more features of metabolic syndrome for 5 years (cryptogenic cirrhosis)
Exclusion Criteria:
* Refusal to consent * Alcohol use \> 14/21 gm/week cutoff * Other causes of chronic liver disease * MELD \> 12 * Hepatic and extrahepatic cancers expected to limit life expectancy \< 2 yrs * prior hepatic resections, TIPS, splenic embolization * prior decompensation events * inability to fit into MRI (failed hula-hoop test) * general contraindication for MRI contrast (GFR \< 30 ml/min) * contraindications for MRI * pregnancy * acute kidney injury * reduced kidney function (GFR \<30ml/min)
OTHER: Standard of care
Nonalcoholic Steatohepatitis
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Study Locations

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Location Contacts
Mayo Clinic in Rochester Rochester, Minnesota Christopher Kigongo - (Kigongo.Christopher@mayo.edu) Mia Mahmoud - (Mahmoud.Mia@mayo.edu)
Virginia Commonwealth University Richmond, Virginia Mohammad Siddiqui, MD - (mohammad.siddiqui@vcuhealth.org)

Oesophageal Protection Study: A Multicentre Study. (IMPACT II)

Patrick Shanley, MS - pshanley@attune-medical.com

NCT04577859
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Inclusion Criteria:
• All AF patients deemed suitable for AF ablation treatment (under general anaesthetic) as per international guidelines and the patient has already decided on AF ablation treatment and are waiting for this procedure.
Exclusion Criteria:

• Inability to consent for any reason.
• Inability to have the endoscopy follow up for any reason.
• Those in extremities of age (<18 or >85) will not be recruited.
• Those with a history of upper gastrointestinal tract bleeding or at risk of trauma e.g. esophageal varices or stricture which means there is a contraindication for instrumentation of the esophagus for any reason during the ablation.
Device: ensoETM. Esophageal cooling during AF ablation, Device: Esophageal temperature monitoring probe
AF - Atrial Fibrillation, Complication, Atrio-Esophageal Fistula
AF ablation, Radiofrequency, Esophageal thermal injury, atrio-esophageal fistula, Esophageal protection, Esophageal cooling, Esophageal temperature monitoring probe
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Study Locations

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Location Contacts
Beth Israel Deaconess Medical Center Boston, Massachusetts Jenifer Kaufman, RN, MS - (jmkaufma@bidmc.harvard.edu)
St.George's Hospital London, Mark M Gallagher, MD - (mark_m_gallagher@hotmail.com)
Texas Cardiac Arrhythmia Research Foundation Austin, Texas Deb Cardinal, RN
University of Colorado Aurora, Colorado
University of Pennsylvania Philadelphia, Pennsylvania Tiffany Sharksoski, BA - (Tiffany.Sharkoski@pennmedicine.upenn.edu)
Virginia Commonwealth University Richmond, Virginia Melissa Sears, MSN, CCRP - (melissa.sears@vcuhealth.org)

BiCaZO: A Study Combining Two Immunotherapies (Cabozantinib and Nivolumab) to Treat Patients With Advanced Melanoma or Squamous Cell Head and Neck Cancer, an immunoMATCH Pilot Study

ctrrecruit@vcu.edu

NCT05136196
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Inclusion Criteria:
* STEP 1 - SPECIMEN SUBMISSION * Participants must have histologically confirmed melanoma that is stage III or IV, unresectable, recurrent, or metastatic non-uveal melanoma OR Participants must have histologically confirmed squamous cell carcinoma of the head and neck (HNSCC) that is either locally recurrent and non-amendable to curative therapy (e.g., radiation, surgery) or metastatic. The primary tumor location must be the oropharynx, oral cavity, hypopharynx, or larynx. Primary tumor site of nasopharynx (any histology) or unknown primary tumor are not eligible * Note: For participants with primary oropharyngeal cancer, human papillomavirus (HPV) or p16 status must be known prior to step 1 registration * Participants must have disease presentation consistent with measurable disease. Note: Current disease measurements will not be required until step 2 registration * Participants must have had documented progression during or within 12 weeks after the last dose of PD-1 checkpoint inhibition-based therapy. Participants must have been receiving checkpoint inhibition for a minimum of 6 weeks. Participants who recur during adjuvant anti-PD1 treatment or within 12 weeks of completion of adjuvant anti-PD1 treatment are eligible if they have measurable disease and are considered unresectable * Participants with known human immunodeficiency virus (HIV)-infection must be receiving anti-retroviral therapy and have an undetectable viral load test within 6 months prior to step 1 registration * Participants with evidence of chronic hepatitis B virus (HBV) infection must have undetectable HBV viral load within 28 days prior to step 1 registration * Participants with a history of hepatitis C virus (HCV) infection must have no detectable viral load within 28 days prior to step 1 registration * Participants must not have an active infection requiring systemic therapy (except HBV, HCV or HIV as mentioned above) * Participants must not have experienced myocardial infarction or thromboembolic event requiring anticoagulation within 90 days prior to step 1 registration, unless clinically stable with ongoing medical management * Participants must have recovered to baseline or =\< grade 1 Common Terminology Criteria for Adverse Events (CTCAE) version (v) 5 toxicities related to any prior treatments, unless adverse events are deemed clinically nonsignificant by the treating investigator or stable on supportive therapy * Participants must not have received more than one prior primary radiotherapy regimen, curative or adjuvant, to the mucosal surfaces of the head and neck, with the additional following criteria: * If the primary radiation is combined with chemotherapy, a minimum of 16 weeks will be required to have elapsed between the end of radiotherapy and step 1 registration. If the radiation is given alone, a minimum of 8 weeks will be required to have elapsed between the end of radiotherapy and step 1 registration * Additional palliative radiotherapy regimens are permitted but cannot have been administered to previously treated tissue (i.e., overlapping fields are excluded) with the exception of central nervous system (CNS) radiation and must be completed at least 4 weeks prior to step 1 registration * Treatment areas should be healed with no sequelae from radiation therapy (RT) that would predispose to fistula formation * Participants must not have received prior treatment with anti-VEGF therapies for any reason * Participants must be \>= 18 years of age * Participants must have a Zubrod Performance Status 0 or 1 * Participants must have adequate cardiac function. Participants with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, must have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification and must be class 2B or better to be eligible for this trial * Participants must not have any known significant organ disfunction that, in the opinion of the treating investigator, may impact suitability for receiving combination nivolumab/cabozantinib treatment * Participants must be able to take oral medication without breaking, opening, crushing, dissolving or chewing capsules * Participants must not have malabsorption syndrome * Participants must not have active autoimmune disease requiring systemic steroids (equivalent of \> 10mg of prednisone) or other immune suppression. Exceptions: * Type 1 diabetes mellitus * Endocrinopathy only requiring hormone replacement * Skin disorders (e.g., vitiligo, psoriasis, or alopecia) not requiring systemic treatment * Conditions not expected to recur in the absence of an external trigger * Participants must not have received an organ allograft * Participants must not have a history of hemoptysis (defined as \>= 1/2 tsp of bright red blood per day) or tumor bleeding within 90 days prior to step 1 registration * Participants must not have any of the following criteria due to the possibility of increased risk for tumor bleeding with cabozantinib therapy: * Prior carotid bleeding * Tumors that invade major vessels (e.g., the carotid) as shown unequivocally by imaging studies * Central (e.g., within 2 cm from the hilum) lung metastases that are cavitary as shown unequivocally by imaging studies * Any prior history of bleeding related to the current head and neck cancer * History of gross hemoptysis (bright red blood of 1/2 teaspoon or more per episode of coughing) within 3 months * Participants must not require concomitant anticoagulation with coumarin agents (e.g., warfarin), direct thrombin inhibitors (e.g., dabigatran), direct factor Xa inhibitor betrixaban, or platelet inhibitors (e.g., clopidogrel) * Participants must not require anticoagulants except for the following: * Prophylactic use of low-dose aspirin for cardio-protection (per local applicable guidelines) and low-dose low molecular weight heparins (LMWH). * Therapeutic doses of LMWH or anticoagulation with direct factor Xa inhibitors, rivaroxaban, edoxaban, or apixaban in participants without known brain metastases who are on a stable dose of the anticoagulant for at least 1 week prior to step 1 registration without clinically significant hemorrhagic complications from the anticoagulation regimen or the tumor * Participants must not have evidence of preexisting uncontrolled hypertension 28 days prior to step 1 registration as documented by baseline blood pressure reading with systolic blood pressure \> 150 mmHg and/or diastolic blood pressure \> 90 mmHg. Participants on antihypertensive therapies with controlled blood pressure are eligible * Participants must not have a prior or concurrent malignancy whose natural history or treatment (in the opinion of the treating physician) has the potential to interfere with the safety or efficacy assessment of the investigational regimen * Participants must not be pregnant or nursing due to the known safety profiles of the drugs in this study. Individuals who are of reproductive potential must have agreed to use an effective contraceptive method with details provided as a part of the consent process. A person who has had menses at any time in the preceding 12 consecutive months or who has semen likely to contain sperm is considered to be of "reproductive potential". In addition to routine contraceptive methods, "effective contraception" also includes refraining from sexual activity that might result in pregnancy and surgery intended to prevent pregnancy (or with a side-effect of pregnancy prevention) including hysterectomy, bilateral oophorectomy, bilateral tubal ligation/occlusion and vasectomy with testing showing no sperm in the semen * Have an adequate archival tissue specimen verified by the local pathologist and documented on the Pathology Review Form from a procedure obtained after the development of resistance to anti-PD-1/L1 therapy. Archival tissue must consist of tumor block or at least 1 hematoxylin and eosin (H\&E)-stained 4-5 micron slide and 20 freshly cut serially sectioned and numbered 4-5 micron unstained, uncharged slides OR Be willing to undergo research biopsy AND have tumor accessible for biopsy based on the following criteria: * Mediastinal, laparoscopic, gastrointestinal, or bronchial endoscopic biopsies can be obtained incidentally to a clinically necessary procedure and NOT for the sole purpose of the clinical trial * Acceptable biopsy procedures are: * Percutaneous biopsy with local anesthetic and/or sedation with an expected risk of severe complications \< 2% * Direct transoral biopsy (with or without local anesthetic and/or sedation) with an expected risk of severe complications \< 2% * Excisional cutaneous biopsy with local anesthetic and/or sedation with an expected risk of severe complications \< 2% * Biopsy with removal of additional tumor tissue during a medically necessary mediastinoscopy, laparoscopy, gastrointestinal endoscopy, bronchoscopy or craniotomy. No open surgical, laparoscopic or endoscopic procedure should be performed solely to obtain a biopsy for this protocol * Removal of additional tumor tissue during a medically necessary surgical procedure * Participants must submit whole blood for germline genomic analysis * Participants must have been offered the opportunity to participate in specimen banking * Note: As a part of the Oncology Patient Enrollment Network (OPEN) registration process the treating institution's identity is provided in order to ensure that the current (within 365 days) date of institutional review board approval for this study has been entered in the system * Participants must be informed of the investigational nature of this study and must sign and give informed consent in accordance with institutional and federal guidelines * Participants with impaired decision-making capacity are eligible as long as their neurological or psychological condition does not preclude their safe participation in the study (e.g., tracking pill consumption and reporting adverse events to the investigator) * STEP 2 TREATMENT REGISTRATION * Note: No tests or exams are required to be repeated for step 2 registration (Treatment). However, participants who are known to have a change in eligibility status after step 1 registration are not eligible for step 2 registration * Participants must continue to meet eligibility for step 1 registration prior to step 2 registration * Participants must have had their tumor tissue submitted via the Southwest Oncology Group (SWOG) Specimen Tracking System prior to step 2 registration * Participants registered during stage II of the protocol must have received assignment to an open cohort from the SWOG Statistics and Data Management Center based on their biomarker screening profile (not applicable for patients registered during stage I of the protocol) * Participants must have measurable disease. All measurable disease must be assessed within 28 days prior to step 2 registration. All non-measurable disease must be assessed within 42 days prior to step 2 registration. Note: All disease must be assessed and documented on the Baseline Tumor Assessment Form (Response Evaluation Criteria in Solid Tumors \[RECIST\] 1.1) * For melanoma participants, CT chest, abdomen and pelvis must be obtained. For HNSCC participants, CT neck and chest must be obtained. Further imaging (i.e., MR brain, CT abdomen/pelvis or extremities, bone scan) will be performed as deemed appropriate by the treating physician * Participants with treated brain metastases must have no evidence of progression on the follow-up brain imaging after central nervous system (CNS)-directed therapy * Participants must not have experienced any significant health changes that, in the opinion of the treating investigator, may impact continued suitability for receiving combination nivolumab/cabozantinib treatment * Participants with treated brain metastases must have discontinued steroid treatment at least 14 days prior to step 2 registration * Participants must not have received investigational agents or monoclonal antibodies (except Food and Drug Administration \[FDA\] approved supportive care antibodies, such as denosumab) within 28 days prior to step 2 registration * Participants must not have received surgery, chemotherapy, radiation therapy, biologic agents, or steroids within 14 days prior to step 2 registration * Participants must not have received administration of a live, attenuated vaccine within 30 days prior to step 2 registration. Note: Participants may have received a messenger ribonucleic acid (mRNA) or viral vector-based coronavirus disease 2019 (COVID-19) vaccine within 30 days prior to step 2 registration * Participants must not have received administration of any strong CYP3A4 inducers, such as but not limited to rifampin, carbamazepine, enzalutamide, mitotane, phenytoin and St. John's wort, within 14 days prior to step 2 registration * Participants must not have received administration of any strong CYP3A4 inhibitors, such as but not limited to clarithromycin, itraconazole, ketoconazole, grapefruit juice, indinavir, nelfinavir, ritonavir, nefazodone, saquinavir, and telithromycin, within 5 times the half-life of the CYP3A inhibitor prior to step 2 registration * Participants must have a history and physical examination performed within 28 days prior to step 2 registration * Leukocytes \>= 3,000/uL (within 28 days prior to step 2 registration) * Absolute neutrophil count \>= 1,500/uL (within 28 days prior to step 2 registration) * Platelets \>= 100,000/uL (within 28 days prior to step 2 registration) * Total bilirubin =\< 1.5 x institutional upper limit of normal (ULN) or =\< 3 x ULN for participants with Gilbert's disease (within 28 days prior to step 2 registration) * Aspartate aminotransferase (AST) =\< 3 x institutional ULN (within 28 days prior to step 2 registration) * Alanine aminotransferase (ALT) =\< 3 x institutional ULN (within 28 days prior to step 2 registration) * Urinalysis: For baseline value (no required value for eligibility) * Measured (OR calculated) creatinine clearance \>= 30 mL/min using the following Cockcroft-Gault Formula. This specimen must have been drawn and processed within 28 days prior to step 2 registration
PROCEDURE: Biopsy Procedure, PROCEDURE: Biospecimen Collection, DRUG: Cabozantinib S-malate, PROCEDURE: Computed Tomography, PROCEDURE: Magnetic Resonance Imaging, BIOLOGICAL: Nivolumab
Clinical Stage III Cutaneous Melanoma AJCC v8, Clinical Stage III HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8, Clinical Stage IV Cutaneous Melanoma AJCC v8, Clinical Stage IV HPV-Mediated (p16-Positive) Oropharyngeal Carcinoma AJCC v8, Locally Recurrent Head and Neck Squamous Cell Carcinoma, Locally Recurrent Hypopharyngeal Squamous Cell Carcinoma, Locally Recurrent Laryngeal Squamous Cell Carcinoma, Locally Recurrent Oral Cavity Squamous Cell Carcinoma, Locally Recurrent Oropharyngeal Squamous Cell Carcinoma, Metastatic Head and Neck Squamous Cell Carcinoma, Metastatic Hypopharyngeal Squamous Cell Carcinoma, Metastatic Laryngeal Squamous Cell Carcinoma, Metastatic Melanoma, Metastatic Oral Cavity Squamous Cell Carcinoma, Metastatic Oropharyngeal Squamous Cell Carcinoma, Recurrent Melanoma, Stage III Hypopharyngeal Carcinoma AJCC v8, Stage III Laryngeal Cancer AJCC v8, Stage III Lip and Oral Cavity Cancer AJCC v8, Stage III Oropharyngeal (p16-Negative) Carcinoma AJCC v8, Stage IV Hypopharyngeal Carcinoma AJCC v8, Stage IV Laryngeal Cancer AJCC v8, Stage IV Lip and Oral Cavity Cancer AJCC v8, Stage IV Oropharyngeal (p16-Negative) Carcinoma AJCC v8, Unresectable Melanoma
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Study Locations

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Location Contacts
Abbott-Northwestern Hospital Minneapolis, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Asplundh Cancer Pavilion Willow Grove, Pennsylvania
Atrium Medical Center-Middletown Regional Hospital Franklin, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Baystate Medical Center Springfield, Massachusetts Site Public Contact - (tamara.wrenn@baystatehealth.org)
Beacon Kalamazoo Cancer Center Kalamazoo, Michigan
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Testing the Addition of Herceptin Hylecta or Phesgo to the Usual Chemotherapy for HER2 Positive Endometrial Serous Carcinoma or Carcinosarcoma

ctrrecruit@vcu.edu

NCT05256225
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Inclusion Criteria:
* Federation of Gynecology and Obstetrics (FIGO) 2009 stage IA-IVB, non-recurrent, chemotherapy (chemo)-naive, HER2-positive endometrial cancer. The following endometrial cancer types are eligible: * Serous * Other endometrial cancers (including clear cell, endometrioid, mixed epithelial, dedifferentiated/undifferentiated) * Carcinosarcoma * NOTE: Endometrial cancers that are mismatch repair deficient (dMMR) by IHC are not eligible * Histologic confirmation of the original primary tumor is required. Submission of surgical pathology report (or endometrial biopsy pathology report in patients who never undergo hysterectomy) is required * Patients must be within 8 weeks of primary surgery (or endometrial biopsy in patients who never undergo hysterectomy) at the time of study registration * Patients may have measurable disease, non-measurable disease, or no measurable disease. In patients with measurable disease, lesions will be defined and monitored by RECIST v 1.1. Measurable disease is defined as at least one lesion that can be accurately measured in at least one dimension (longest diameter to be recorded). Each lesion must be \>= 10 mm when measured by CT or magnetic resonance imaging (MRI). Lymph nodes must be \>= 15 mm in short axis when measured by CT or MRI * For patients with uterine-confined (stage I) disease, the tumor must be invasive into the myometrium. Any amount of myoinvasion is acceptable for eligibility. Patients with non-invasive disease, endometrial intraepithelial carcinoma alone, or disease confined to a polyp will be excluded * All patients must have tumors that are HER2 positive as defined by American Society of Clinical Oncology (ASCO)/College of American Pathologists (CAP) 2018 Breast Cancer guidelines. IHC and ISH testing will be done locally, at each participating institution and interpreted by local pathologists. In general HER2 positivity is defined as any of the following: * 3+ immunohistochemistry (IHC), * 2+ IHC with positive in situ hybridization (ISH) Alternatively, patients could be eligible if next generation sequencing (NGS) demonstrates HER2 (ERBB2) amplification. NGS testing can be performed through any designated labs as per the National Cancer Institute (NCI) MATCH/NCI Combo-MATCH trial. Pathology report showing results of institutional HER2 testing (or NGS testing results) must be submitted. Sites must submit all results available (IHC, ISH, and NGS) * Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1 or 2 * Age \>= 18 * Platelets \>= 100,000/mcl (within 14 days prior to registration) * Absolute neutrophil count (ANC) \>= 1,500/mcl (within 14 days prior to registration) * Creatinine =\< 1.5 x institutional/laboratory upper limit of normal (ULN) or estimated Glomerular filtration rate (eGFR) \>= 50 mL/min using either the Cockcroft-Gault equation, the Modification of Diet in Renal Disease Study, or as reported in the comprehensive metabolic panel/basic metabolic panel (eGFR) (within 14 days prior to registration) * Total serum bilirubin level =\< 1.5 x ULN (patients with known Gilbert's disease who have bilirubin level =\< 3 x ULN may be enrolled) (within 14 days prior to registration) * Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =\< 3 x ULN (within 14 days prior to registration) * Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months of registration are eligible for this trial * Although the uterus will have been removed in the vast majority of patients, for patients of child-bearing potential: negative urine or serum pregnancy test. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test is required. Patients will be considered of non-reproductive potential if they are either: * Postmenopausal (defined as at least 12 months with no menses without an alternative medical cause; in women \< 45 years of age, a high follicle stimulating hormone \[FSH\] level in the postmenopausal range may be used to confirm a postmenopausal state in women not using hormonal contraception or hormonal replacement therapy. In the absence of 12 months of amenorrhea, a single FSH measurement is insufficient); OR * Have had a hysterectomy and/or bilateral oophorectomy, bilateral salpingectomy or bilateral tubal ligation/occlusion at least 6 weeks prior to registration * Have a congenital or acquired condition that prevents childbearing * Patients with a prior or concurrent malignancy whose natural history or treatment does not have the potential to interfere with the safety or efficacy assessment of the investigational regimen are eligible for this trial * Patients with evidence of chronic hepatitis B virus (HBV) infection must have an undetectable HBV viral load on suppressive therapy, if indicated * Patients with a history of hepatitis C virus (HCV) infection must have been treated and cured. For patients with HCV infection who are currently on treatment, they are eligible if they have an undetectable HCV viral load * Patients with treated brain metastases are eligible if follow-up brain imaging after central nervous system (CNS)-directed therapy shows no evidence of progression * The patient or a legally authorized representative must provide study-specific informed consent prior to study entry and, for patients treated in the United States (U.S.), authorization permitting release of personal health information
Exclusion Criteria:
* Prior Therapy: * Patients must NOT have received prior chemotherapy, biologic therapy, or targeted therapy for treatment of endometrial carcinoma * Patients must NOT have received prior radiation therapy for treatment of endometrial carcinoma. Prior radiation includes external beam pelvic radiation therapy, external beam extended field pelvic/para-aortic radiation therapy, and/or intravaginal brachytherapy * NOTE: Vaginal brachytherapy for treatment of endometrial cancer is permitted during study treatment. Planned use of vaginal brachytherapy must be declared at time of registration * Patients may have received prior hormonal therapy for treatment of endometrial carcinoma. All hormonal therapy must be discontinued at least one week prior to registration * Patients may not have a planned interval cytoreduction or hysterectomy, prior to documentation of progression, after study registration * Patients may not have planned external beam radiotherapy, prior to documentation of progression, after study registration * Significant cardiovascular disease including: * Uncontrolled hypertension, defined as systolic \> 150 mm Hg or diastolic \> 90 mm Hg despite antihypertensive medications * Myocardial infarction or unstable angina within 6 months prior to registration * New York Heart Association functional classification II, III or IV * Serious cardiac arrhythmia requiring medication. This does not include asymptomatic, atrial fibrillation with controlled ventricular rate * Significant lung disease: dyspnea at rest grade 2 or greater (resulting from extensive tumor involvement or other causes), pneumonitis grade 2 or greater, interstitial lung disease grade 2 or greater, idiopathic pulmonary fibrosis, cystic fibrosis, Aspergillosis, active tuberculosis, or history of opportunistic infections (pneumocystis pneumonia or cytomegalovirus pneumonia) * Patients with uncontrolled intercurrent illness including, but not limited to: ongoing or active infection (except for uncomplicated urinary tract infection), uncontrolled interstitial lung disease, symptomatic congestive heart failure, or psychiatric illness/social situations that would limit compliance with study requirements * Treatment with strong CYP2C8 or CYP3A4 inhibitors or inducers within 14 days or 5 drug-elimination half-lives, whichever is longer, prior to registration * Women who are unwilling to discontinue nursing
PROCEDURE: Biospecimen Collection, DRUG: Carboplatin, PROCEDURE: Computed Tomography, PROCEDURE: Echocardiography Test, RADIATION: High-Dose-Rate Vaginal Cuff Brachytherapy, DRUG: Hyaluronidase-zzxf/Pertuzumab/Trastuzumab, PROCEDURE: Multigated Acquisition Scan, DRUG: Paclitaxel, OTHER: Survey Administration, DRUG: Trastuzumab/Hyaluronidase-oysk
Endometrial Carcinoma, Endometrial Clear Cell Adenocarcinoma, Endometrial Dedifferentiated Carcinoma, Endometrial Endometrioid Adenocarcinoma, Endometrial Mixed Cell Adenocarcinoma, Endometrial Serous Adenocarcinoma, Endometrial Undifferentiated Carcinoma, Uterine Corpus Malignant Mixed Mesodermal (Mullerian) Tumor
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Location Contacts
Abbott-Northwestern Hospital Minneapolis, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Adena Regional Medical Center Chillicothe, Ohio Site Public Contact - (Jeffh@columbusccop.org)
AdventHealth Orlando Apopka, Florida Site Public Contact - (FH.Cancer.Research@flhosp.org)
AdventHealth Porter Denver, Colorado Site Public Contact - (research.institute@adventhealth.com)
Alaska Women's Cancer Care Anchorage, Alaska Site Public Contact - (AKPAMC.OncologyResearchSupport@providence.org)
Alegent Health Bergan Mercy Medical Center Omaha, Nebraska Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Alta Bates Summit Medical Center-Herrick Campus Berkeley, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Ascension Saint Vincent Indianapolis Hospital Indianapolis, Indiana
Asplundh Cancer Pavilion Willow Grove, Pennsylvania Site Public Contact - (ONCTrialNow@jefferson.edu)
Atrium Medical Center-Middletown Regional Hospital Franklin, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Augusta University Medical Center Augusta, Georgia Site Public Contact - (ga_cares@augusta.edu)
Aultman Health Foundation Canton, Ohio Site Public Contact - (ClinicalReserachDept@aultman.com)
Avera Cancer Institute Sioux Falls, South Dakota Site Public Contact - (OncRegulatory@avera.org)
Avera Cancer Institute at Marshall Marshall, Minnesota Site Public Contact - (OncRegulatory@avera.org)
Avera Cancer Institute-Aberdeen Aberdeen, South Dakota Site Public Contact - (oncregulatory@avera.org)
Banner North Colorado Medical Center Greeley, Colorado Site Public Contact - (BMDACCResearchCOMailbox@bannerhealth.com)
Banner North Colorado Medical Center - Loveland Campus Loveland, Colorado Site Public Contact - (BMDACCResearchCOMailbox@bannerhealth.com)
Banner University Medical Center - Tucson Tucson, Arizona Site Public Contact - (UACC-IIT@uacc.arizona.edu)
Baptist Health Lexington Lexington, Kentucky
Baptist Health Louisville Louisville, Kentucky
Baystate Medical Center Springfield, Massachusetts Site Public Contact - (tamara.wrenn@baystatehealth.org)
Beacon Kalamazoo Cancer Center Kalamazoo, Michigan
Benefis Sletten Cancer Institute Great Falls, Montana Site Public Contact - (mccinfo@mtcancer.org)
Billings Clinic Cancer Center Billings, Montana Site Public Contact - (research@billingsclinic.org)
Bozeman Health Deaconess Hospital Bozeman, Montana Site Public Contact - (mccinfo@mtcancer.org)
Bronson Battle Creek Battle Creek, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Bronson Methodist Hospital Kalamazoo, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Broward Health Medical Center Fort Lauderdale, Florida Site Public Contact - (Allison.bruce@nemours.org)
Bryn Mawr Hospital Bryn Mawr, Pennsylvania Site Public Contact - (turzoe@mlhs.org)
California Pacific Medical Center-Pacific Campus San Francisco, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Cancer Care Center of O'Fallon O'Fallon, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Care Specialists of Illinois - Decatur Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Center of Western Wisconsin New Richmond, Wisconsin Site Public Contact - (mmcorc@healthpartners.com)
Cancer Hematology Centers - Flint Flint, Michigan Site Public Contact - (wstrong@ghci.org)
Cancer and Hematology Centers of Western Michigan - Norton Shores Norton Shores, Michigan Site Public Contact - (connie.szczepanek@crcwm.org)
Carilion Roanoke Memorial Hospital Roanoke, Virginia
Carle Cancer Center Urbana, Illinois Site Public Contact - (Research@carle.com)
Carle Cancer Institute Normal Normal, Illinois Site Public Contact - (Research@Carle.com)
Carle Physician Group-Effingham Effingham, Illinois Site Public Contact - (Research@carle.com)
Carle Physician Group-Mattoon/Charleston Mattoon, Illinois Site Public Contact - (Research@carle.com)
Carle at The Riverfront Danville, Illinois Site Public Contact - (Research@Carle.com)
Case Western Reserve University Cleveland, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
Centralia Oncology Clinic Centralia, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Centro Comprensivo de Cancer de UPR San Juan, Site Public Contact - (Roster@nrgoncology.org)
Chester County Hospital West Chester, Pennsylvania
City of Hope Comprehensive Cancer Center Duarte, California
City of Hope Seacliff Huntington Beach, California
City of Hope Upland Upland, California
City of Hope at Irvine Lennar Irvine, California
City of Hope at Long Beach Elm Long Beach, California
Community Hospital of Anaconda Anaconda, Montana Site Public Contact - (mccinfo@mtcancer.org)
Community Medical Center Missoula, Montana Site Public Contact - (mccinfo@mtcancer.org)
Community Medical Center Missoula, Montana Site Public Contact - (Lennette.Gonzales@rwjbh.org)
Cooper Hospital University Medical Center Camden, New Jersey
Corewell Health Beaumont Troy Hospital Troy, Michigan
Corewell Health Farmington Hills Hospital Farmington Hills, Michigan
Corewell Health Grand Rapids Hospitals - Butterworth Hospital Grand Rapids, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center Saint Joseph, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health Lakeland Hospitals - Niles Hospital Niles, Michigan
Corewell Health Lakeland Hospitals - Saint Joseph Hospital Saint Joseph, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health Reed City Hospital Reed City, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health William Beaumont University Hospital Royal Oak, Michigan
CoxHealth South Hospital Springfield, Missouri
Crossroads Cancer Center Effingham, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Danbury Hospital Danbury, Connecticut
Decatur Memorial Hospital Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Dell Seton Medical Center at The University of Texas Austin, Texas
Duke Cancer Center Cary Cary, North Carolina Site Public Contact - (NCTNStudyTeam@dm.duke.edu)
Duke University Medical Center Durham, North Carolina
Duke Women's Cancer Care Raleigh Raleigh, North Carolina
ECU Health Medical Center Greenville, North Carolina Site Public Contact - (research@ecuhealth.org)
East Jefferson General Hospital Metairie, Louisiana Site Public Contact - (emede1@lsuhsc.edu)
Emory Decatur Hospital Decatur, Georgia Site Public Contact - (clinicaltrialsoncology@dekalbmedical.org)
Emory Saint Joseph's Hospital Atlanta, Georgia
Emory University Hospital Midtown Atlanta, Georgia
Emory University Hospital/Winship Cancer Institute Atlanta, Georgia
Fairfield Medical Center Lancaster, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Fairview Southdale Hospital Edina, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
First Physicians Group-Sarasota Sarasota, Florida
Florida Cancer Specialists - Sarasota Downtown Sarasota, Florida
Florida Cancer Specialists - Venice Pinebrook Venice, Florida Site Public Contact - (ClinicalTrials@FLCancer.com)
Forbes Hospital Monroeville, Pennsylvania
Fox Chase Cancer Center Philadelphia, Pennsylvania
Franciscan Health Indianapolis Indianapolis, Indiana
Franciscan Health Mooresville Mooresville, Indiana
Franciscan Saint Elizabeth Health - Lafayette East Lafayette, Indiana Site Public Contact - (ctsucontact@westat.com)
Gangnam Severance Hospital Seoul,
Geauga Hospital Chardon, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
Genesee Hematology Oncology PC Flint, Michigan
Genesis Healthcare System Cancer Care Center Zanesville, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Genesys Hurley Cancer Institute Flint, Michigan Site Public Contact - (wstrong@ghci.org)
George Washington University Medical Center Washington D.C., District of Columbia
Good Samaritan Hospital - Cincinnati Cincinnati, Ohio Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Goshen Center for Cancer Care Goshen, Indiana Site Public Contact - (cccois@goshenhealth.com)
Grady Health System Atlanta, Georgia
Grand Valley Oncology Grand Junction, Colorado Site Public Contact - (gvoclinicaltrials@gjhosp.org)
Greater Baltimore Medical Center Baltimore, Maryland
Gundersen Lutheran Medical Center La Crosse, Wisconsin Site Public Contact - (cancerctr@gundersenhealth.org)
Hackensack University Medical Center Hackensack, New Jersey
Harold Alfond Center for Cancer Care Augusta, Maine
Hayworth Cancer Center High Point, North Carolina
Heartland Oncology and Hematology LLP Council Bluffs, Iowa
Helen F Graham Cancer Center Newark, Delaware Site Public Contact - (lbarone@christianacare.org)
Henrico Doctor's Hospital Richmond, Virginia
Houston Methodist Hospital Houston, Texas
Houston Methodist Saint John Hospital Nassau Bay, Texas Site Public Contact - (Roster@nrgoncology.org)
Houston Methodist Sugar Land Hospital Sugar Land, Texas
Houston Methodist The Woodlands Hospital Shenandoah, Texas Site Public Contact - (hmthewoodlands@houstonmethodist.org)
Houston Methodist West Hospital Houston, Texas
Huntsman Cancer Institute/University of Utah Salt Lake City, Utah Site Public Contact - (cancerinfo@hci.utah.edu)
Hurley Medical Center Flint, Michigan Site Public Contact - (wstrong@ghci.org)
IU Health North Hospital Carmel, Indiana Site Public Contact - (iutrials@iu.edu)
Indiana University/Melvin and Bren Simon Cancer Center Indianapolis, Indiana Site Public Contact - (iutrials@iu.edu)
Ingalls Memorial Hospital Harvey, Illinois Site Public Contact - (clinicaltrials@ingalls.org)
Intermountain Health West End Clinic Billings, Montana
Jefferson Hospital Jefferson Hills, Pennsylvania
Jersey Shore Medical Center Neptune City, New Jersey
John H Stroger Jr Hospital of Cook County Chicago, Illinois
John Muir Medical Center-Concord Concord, California
John Muir Medical Center-Walnut Creek Walnut Creek, California Site Public Contact - (clinicalresearch@johnmuirhealth.com)
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore, Maryland Site Public Contact - (jhcccro@jhmi.edu)
Jupiter Medical Center Jupiter, Florida
Kaiser Permanente - Panorama City Panorama City, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente Los Angeles Medical Center Los Angeles, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Irvine Irvine, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Riverside Riverside, California Site Public Contact - (clinical.trials@kp.org)
Kapiolani Medical Center for Women and Children Honolulu, Hawaii
Keimyung University-Dongsan Medical Center Dalseo-gu, Daegu Site Public Contact - (ho@dsmc.or.kr)
Knox Community Hospital Mount Vernon, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Kootenai Clinic Cancer Services - Post Falls Post Falls, Idaho Site Public Contact - (mccinfo@mtcancer.org)
Kootenai Clinic Cancer Services - Sandpoint Sandpoint, Idaho Site Public Contact - (mccinfo@mtcancer.org)
Kootenai Health - Coeur d'Alene Coeur d'Alene, Idaho Site Public Contact - (mccinfo@mtcancer.org)
LSU Health Baton Rouge-North Clinic Baton Rouge, Louisiana Site Public Contact - (research@ololrmc.com)
LSU Healthcare Network / Metairie Multi-Specialty Clinic Metairie, Louisiana Site Public Contact - (emede1@lsuhsc.edu)
Lankenau Medical Center Wynnewood, Pennsylvania Site Public Contact - (turzoe@mlhs.org)
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York, New York Site Public Contact - (CancerTrials@nyulangone.org)
Legacy Good Samaritan Hospital and Medical Center Portland, Oregon Site Public Contact - (cancer@lhs.org)
Legacy Meridian Park Hospital Tualatin, Oregon
Legacy Salmon Creek Hospital Vancouver, Washington
Lehigh Valley Hospital - Muhlenberg Bethlehem, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Lehigh Valley Hospital-Cedar Crest Allentown, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Lehigh Valley Hospital-Hazleton Hazleton, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Lewis Cancer and Research Pavilion at Saint Joseph's/Candler Savannah, Georgia Site Public Contact - (underberga@sjchs.org)
Licking Memorial Hospital Newark, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Logan Health Medical Center Kalispell, Montana Site Public Contact - (mccinfo@mtcancer.org)
MU Health - University Hospital/Ellis Fischel Cancer Center Columbia, Missouri
MaineHealth Maine Medical Center- Scarborough Scarborough, Maine Site Public Contact - (clinicalresearch@mainehealth.org)
Marietta Memorial Hospital Marietta, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Marshfield Medical Center - Minocqua Minocqua, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center - Weston Weston, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-EC Cancer Center Eau Claire, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-Marshfield Marshfield, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-Rice Lake Rice Lake, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-River Region at Stevens Point Stevens Point, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Mary Greeley Medical Center Ames, Iowa
McFarland Clinic - Ames Ames, Iowa Site Public Contact - (ksoder@mcfarlandclinic.com)
McFarland Clinic - Boone Boone, Iowa
McFarland Clinic - Jefferson Jefferson, Iowa
McFarland Clinic - Marshalltown Marshalltown, Iowa
McFarland Clinic - Trinity Cancer Center Fort Dodge, Iowa
MedStar Franklin Square Medical Center/Weinberg Cancer Institute Baltimore, Maryland
Medical College of Wisconsin Milwaukee, Wisconsin
Medical Oncology Hematology Consultants PA Newark, Delaware Site Public Contact - (lbarone@christianacare.org)
Medical University of South Carolina Charleston, South Carolina Site Public Contact - (hcc-clinical-trials@musc.edu)
Memorial Hermann Texas Medical Center Houston, Texas
Memorial Hospital Marysville, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Memorial Hospital of South Bend South Bend, Indiana
Memorial Medical Center Modesto, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Memorial Sloan Kettering Basking Ridge Basking Ridge, New Jersey
Memorial Sloan Kettering Bergen Montvale, New Jersey
Memorial Sloan Kettering Cancer Center New York, New York
Memorial Sloan Kettering Commack Commack, New York
Memorial Sloan Kettering Monmouth Middletown, New Jersey
Memorial Sloan Kettering Nassau Uniondale, New York
Memorial Sloan Kettering Westchester Harrison, New York
Mercy Health - Perrysburg Hospital Perrysburg, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Health - Saint Anne Hospital Toledo, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Health - Saint Vincent Hospital Toledo, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Hospital Coon Rapids, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Mercy Hospital Oklahoma City Oklahoma City, Oklahoma
Mercy Hospital Saint Louis St Louis, Missouri
Mercy Hospital South St Louis, Missouri Site Public Contact - (Danielle.Werle@mercy.net)
Methodist Willowbrook Hospital Houston, Texas Site Public Contact - (Roster@nrgoncology.org)
MetroHealth Medical Center Cleveland, Ohio Site Public Contact - (ababal@metrohealth.org)
Miami Valley Cancer Care and Infusion Greenville, Ohio
Miami Valley Hospital Dayton, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Miami Valley Hospital North Englewood, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Miami Valley Hospital South Centerville, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Minnesota Oncology Hematology PA-Maplewood Maplewood, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Minnesota Oncology Hematology PA-Woodbury Woodbury, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Monmouth Medical Center Long Branch, New Jersey Site Public Contact - (mary.danish@rwjbh.org)
Monmouth Medical Center Southern Campus Lakewood, New Jersey Site Public Contact - (mary.danish@rwjbh.org)
Mount Carmel East Hospital Columbus, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mount Carmel Grove City Hospital Grove City, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mount Sinai Chelsea New York, New York Site Public Contact - (CCTO@mssm.edu)
Mount Sinai Hospital New York, New York Site Public Contact - (CCTO@mssm.edu)
Munson Medical Center Traverse City, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
MyMichigan Medical Center Saginaw Saginaw, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
MyMichigan Medical Center Tawas Tawas City, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
NYU Langone Hospital - Long Island Mineola, New York Site Public Contact - (cancertrials@nyulangone.org)
Nebraska Cancer Specialists/Oncology Hematology West PC - MECC Omaha, Nebraska
Nebraska Cancer Specialists/Oncology Hematology West PC - MEJ Council Bluffs, Iowa Site Public Contact - (Liza.brandes@nmhs.org)
Nebraska Methodist Hospital Omaha, Nebraska
NorthShore University HealthSystem-Evanston Hospital Evanston, Illinois
NorthShore University HealthSystem-Glenbrook Hospital Glenview, Illinois
NorthShore University HealthSystem-Highland Park Hospital Highland Park, Illinois
Northwest Cancer Center - Hobart Hobart, Indiana
Northwest Cancer Center - Main Campus Crown Point, Indiana
Northwest Cancer Center - Valparaiso Valparaiso, Indiana Site Public Contact - (CancerResearch@COMHS.org)
Northwest Community Hospital Arlington Heights, Illinois
Northwest Oncology LLC Dyer, Indiana
Northwestern Medicine Cancer Center Delnor Geneva, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Cancer Center Kishwaukee DeKalb, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Cancer Center Warrenville Warrenville, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Glenview Outpatient Center Glenview, Illinois
Northwestern Medicine Grayslake Outpatient Center Grayslake, Illinois
Northwestern Medicine Lake Forest Hospital Lake Forest, Illinois Site Public Contact - (cancertrials@northwestern.edu)
Northwestern Medicine Orland Park Orland Park, Illinois Site Public Contact - (nctnprogram_rhlccc@northwestern.edu)
Northwestern University Chicago, Illinois Site Public Contact - (cancer@northwestern.edu)
Norwalk Hospital Norwalk, Connecticut Site Public Contact - (jennifer.long@norwalkhealth.org)
Novant Health New Hanover Regional Medical Center Wilmington, North Carolina
Ochsner Baptist Medical Center New Orleans, Louisiana Site Public Contact - (Elisemarie.curry@ochsner.org)
Ochsner Hematology Oncology North Shore - Covington (West Region) Covington, Louisiana Site Public Contact - (Cheryl.kesler@ochsner.org)
Ochsner Medical Center Jefferson New Orleans, Louisiana Site Public Contact - (Elisemarie.curry@ochsner.org)
Ohio State University Comprehensive Cancer Center Columbus, Ohio Site Public Contact - (Jamesline@osumc.edu)
Oklahoma Cancer Specialists and Research Institute-Tulsa Tulsa, Oklahoma
Oncology Hematology Associates of Saginaw Valley PC Saginaw, Michigan
OptumCare Cancer Care at Charleston Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
OptumCare Cancer Care at Fort Apache Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
OptumCare Cancer Care at Seven Hills Henderson, Nevada Site Public Contact - (research@sncrf.org)
Oregon Health and Science University Portland, Oregon Site Public Contact - (trials@ohsu.edu)
Our Lady of the Lake Medical Oncology Baton Rouge, Louisiana Site Public Contact - (research@ololrmc.com)
Our Lady of the Lake Physician Group Baton Rouge, Louisiana Site Public Contact - (research@ololrmc.com)
Palo Alto Medical Foundation-Gynecologic Oncology Mountain View, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Palo Alto Medical Foundation-Santa Cruz Santa Cruz, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Palo Alto Medical Foundation-Sunnyvale Sunnyvale, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Paoli Memorial Hospital Paoli, Pennsylvania Site Public Contact - (turzoe@mlhs.org)
Park Nicollet Clinic - Saint Louis Park Saint Louis Park, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Parkland Memorial Hospital Dallas, Texas Site Public Contact - (canceranswerline@UTSouthwestern.edu)
Pennsylvania Hospital Philadelphia, Pennsylvania Site Public Contact - (PMCancerResearch@pennmedicine.upenn.edu)
Phelps Health Delbert Day Cancer Institute Rolla, Missouri Site Public Contact - (research@phelpshealth.org)
Piedmont Hospital Atlanta, Georgia Site Public Contact - (ORS@piedmont.org)
Pocono Medical Center East Stroudsburg, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Presbyterian Kaseman Hospital Albuquerque, New Mexico
Presbyterian Rust Medical Center/Jorgensen Cancer Center Rio Rancho, New Mexico
ProHealth D N Greenwald Center Mukwonago, Wisconsin Site Public Contact - (research.institute@phci.org)
ProHealth Oconomowoc Memorial Hospital Oconomowoc, Wisconsin
ProMedica Flower Hospital Sylvania, Ohio Site Public Contact - (PCIOncResearch@promedica.org)
Providence Cancer Institute Clackamas Clinic Clackamas, Oregon
Providence Newberg Medical Center Newberg, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Providence Portland Medical Center Portland, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Providence Saint Vincent Medical Center Portland, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Queen's Medical Center Honolulu, Hawaii
Rapid City Regional Hospital Rapid City, South Dakota
Regions Hospital Saint Paul, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Riddle Memorial Hospital Media, Pennsylvania Site Public Contact - (turzoe@mlhs.org)
Riverside Methodist Hospital Columbus, Ohio
Riverview Medical Center/Booker Cancer Center Red Bank, New Jersey
Robert Wood Johnson University Hospital Somerset Somerville, New Jersey Site Public Contact - (Siby.Varughese@rwjbh.org)
Rush MD Anderson Cancer Center Chicago, Illinois
Rush-Copley Healthcare Center Yorkville, Illinois Site Public Contact - (Cancer.Research@rushcopley.com)
Rush-Copley Medical Center Aurora, Illinois Site Public Contact - (RCMC_Cancer_Research@rush.edu)
Rutgers Cancer Institute of New Jersey New Brunswick, New Jersey
Rutgers New Jersey Medical School Newark, New Jersey
Saint Alphonsus Cancer Care Center-Boise Boise, Idaho
Saint Alphonsus Cancer Care Center-Caldwell Caldwell, Idaho
Saint Alphonsus Cancer Care Center-Nampa Nampa, Idaho
Saint Alphonsus Cancer Care Center-Ontario Ontario, Oregon
Saint Ann's Hospital Westerville, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Saint Barnabas Medical Center Livingston, New Jersey Site Public Contact - (joanne.loeb@rwjbh.org)
Saint Catherine Hospital Indianapolis, Indiana Site Public Contact - (Roster@nrgoncology.org)
Saint Elizabeth Healthcare Edgewood Edgewood, Kentucky Site Public Contact - (Kristi.Curtsinger@stelizabeth.com)
Saint Joseph Hospital - Orange Orange, California
Saint Joseph's/Candler - Bluffton Campus Bluffton, South Carolina Site Public Contact - (underberga@sjchs.org)
Saint Luke's Cancer Center - Allentown Allentown, Pennsylvania
Saint Luke's Cancer Institute - Boise Boise, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Cancer Institute - Fruitland Fruitland, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Cancer Institute - Meridian Meridian, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Cancer Institute - Nampa Nampa, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Cancer Institute - Twin Falls Twin Falls, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Hospital - Upper Bucks Campus Quakertown, Pennsylvania
Saint Luke's Hospital-Anderson Campus Easton, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
Saint Luke's University Hospital-Bethlehem Campus Bethlehem, Pennsylvania
Saint Mary Medical Center Hobart, Indiana Site Public Contact - (CancerResearch@COMHS.org)
Saint Mary's Oncology/Hematology Associates of West Branch West Branch, Michigan
Saint Patrick Hospital - Community Hospital Missoula, Montana Site Public Contact - (amy.hanneman@providence.org)
Saint Rita's Medical Center Lima, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Saint Vincent Frontier Cancer Center Billings, Montana
Saint Vincent Hospital Erie, Pennsylvania
Saint Vincent Hospital Cancer Center Green Bay Green Bay, Wisconsin Site Public Contact - (WI_research_admin@hshs.org)
Saint Vincent Hospital Cancer Center at Oconto Falls Oconto Falls, Wisconsin Site Public Contact - (WI_research_admin@hshs.org)
Saint Vincent Hospital Cancer Center at Saint Mary's Green Bay, Wisconsin Site Public Contact - (wi_research_admin@hshs.org)
Saint Vincent Hospital Cancer Center at Sheboygan Sheboygan, Wisconsin Site Public Contact - (wi_research_admin@hshs.org)
Saint Vincent Hospital Cancer Center at Sturgeon Bay Sturgeon Bay, Wisconsin Site Public Contact - (wi_research_admin@hshs.org)
Samsung Changwon Hospital Seoul, Gyeongsangnam-do
Sanford Bismarck Medical Center Bismarck, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Broadway Medical Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Cancer Center Oncology Clinic Sioux Falls, South Dakota Site Public Contact - (OncologyClinicTrialsSF@sanfordhealth.org)
Sanford Roger Maris Cancer Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford USD Medical Center - Sioux Falls Sioux Falls, South Dakota Site Public Contact - (OncologyClinicalTrialsSF@SanfordHealth.org)
Sarasota Memorial Hospital Sarasota, Florida
Sarasota Memorial Hospital-Venice N. Venice, Florida
Seoul National University Bundang Hospital Seongnam-si, Gyeonggi-do
Sheboygan Physicians Group Sheboygan, Wisconsin Site Public Contact - (wi_research_admin@hshs.org)
Sibley Memorial Hospital Washington D.C., District of Columbia Site Public Contact - (jquiver1@jhmi.edu)
Sidney Kimmel Cancer Center Washington Township Sewell, New Jersey Site Public Contact - (ONCTrialNow@jefferson.edu)
Sinai Hospital of Baltimore Baltimore, Maryland
Smilow Cancer Hospital Care Center - Guilford Guilford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center - Waterford Waterford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center - Westerly Westerly, Rhode Island Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Glastonbury Glastonbury, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Greenwich Greenwich, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Long Ridge Stamford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Saint Francis Hartford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center-Fairfield Fairfield, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center-Trumbull Trumbull, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital-Derby Care Center Derby, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital-Torrington Care Center Torrington, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital-Waterbury Care Center Waterbury, Connecticut Site Public Contact - (canceranswers@yale.edu)
South Jordan Health Center South Jordan, Utah Site Public Contact - (cancerinfo@hci.utah.edu)
Southern Illinois University School of Medicine Springfield, Illinois
Southern Ohio Medical Center Portsmouth, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Springfield Clinic Springfield, Illinois
Springfield Memorial Hospital Springfield, Illinois Site Public Contact - (pallante.beth@mhsil.com)
Springfield Regional Cancer Center Springfield, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Springfield Regional Medical Center Springfield, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Stanford Cancer Institute Palo Alto Palo Alto, California Site Public Contact - (ccto-office@stanford.edu)
State University of New York Upstate Medical University Syracuse, New York
Strecker Cancer Center-Belpre Belpre, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Sudarshan K Sharma MD Limited-Gynecologic Oncology Hinsdale, Illinois
Sutter Auburn Faith Hospital Auburn, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Sutter Medical Center Sacramento Sacramento, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Sutter Roseville Medical Center Roseville, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Swedish Cancer Institute-Edmonds Edmonds, Washington Site Public Contact - (PCRC-NCORP@Swedish.org)
Swedish Medical Center-First Hill Seattle, Washington Site Public Contact - (PCRC-NCORP@Swedish.org)
Tarrant County Hospital District/JPS Health Network Fort Worth, Texas Site Public Contact - (macosta02@jpshealth.org)
The Community Hospital Munster, Indiana
The Mark H Zangmeister Center Columbus, Ohio Site Public Contact - (Jeffh@columbusccop.org)
The West Clinic - Wolf River Germantown, Tennessee
Thomas Jefferson University Hospital Philadelphia, Pennsylvania Site Public Contact - (ONCTrialNow@jefferson.edu)
Trinity Health Grand Rapids Hospital Grand Rapids, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Trinity Health IHA Medical Group Hematology Oncology - Brighton Brighton, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health IHA Medical Group Hematology Oncology - Canton Canton, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital Chelsea, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus Ypsilanti, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health Muskegon Hospital Muskegon, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Trinity Health Saint Joseph Mercy Oakland Hospital Pontiac, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health Saint Mary Mercy Livonia Hospital Livonia, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
UC Comprehensive Cancer Center at Silver Cross New Lenox, Illinois Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
UC Irvine Health/Chao Family Comprehensive Cancer Center Orange, California Site Public Contact - (ucstudy@uci.edu)
UCHealth - Cherry Creek Denver, Colorado Site Public Contact - (Roster@nrgoncology.org)
UCHealth Highlands Ranch Hospital Highlands Ranch, Colorado
UCHealth University of Colorado Hospital Aurora, Colorado
UCI Health - Chao Family Comprehensive Cancer Center and Ambulatory Care Irvine, California Site Public Contact - (ucstudy@uci.edu)
UChicago Medicine Northwest Indiana Crown Point, Indiana Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
UH Seidman Cancer Center at Lake Health Mentor Campus Mentor, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
UH Seidman Cancer Center at Saint John Medical Center Westlake, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
UHHS-Chagrin Highlands Medical Center Beachwood, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
UNC Lineberger Comprehensive Cancer Center Chapel Hill, North Carolina Site Public Contact - (cancerclinicaltrials@med.unc.edu)
UT Southwestern Clinical Center at Richardson/Plano Richardson, Texas Site Public Contact - (Suzanne.cole@utsouthwestern.edu)
UT Southwestern/Simmons Cancer Center-Dallas Dallas, Texas Site Public Contact - (canceranswerline@UTSouthwestern.edu)
UT Southwestern/Simmons Cancer Center-Fort Worth Fort Worth, Texas Site Public Contact - (canceranswerline@UTSouthwestern.edu)
UW Cancer Center at ProHealth Care Waukesha, Wisconsin Site Public Contact - (Chanda.miller@phci.org)
UW Health Carbone Cancer Center Rockford Rockford, Illinois Site Public Contact - (lkline@uwhealth.org)
United Hospital Saint Paul, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
University Hospitals Parma Medical Center Parma, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
University Medical Center New Orleans New Orleans, Louisiana Site Public Contact - (emede1@lsuhsc.edu)
University of Alabama at Birmingham Cancer Center Birmingham, Alabama Site Public Contact - (gingerreeves@uabmc.edu)
University of Arizona Cancer Center-North Campus Tucson, Arizona Site Public Contact - (UACC-IIT@uacc.arizona.edu)
University of Arkansas for Medical Sciences Little Rock, Arkansas
University of California Davis Comprehensive Cancer Center Sacramento, California
University of Chicago Comprehensive Cancer Center Chicago, Illinois Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
University of Chicago Medicine-Orland Park Orland Park, Illinois Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
University of Iowa/Holden Comprehensive Cancer Center Iowa City, Iowa
University of Michigan Health - West Wyoming, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
University of Michigan Rogel Cancer Center Ann Arbor, Michigan Site Public Contact - (CancerAnswerLine@med.umich.edu)
University of Minnesota/Masonic Cancer Center Minneapolis, Minnesota
University of Nebraska Medical Center Omaha, Nebraska Site Public Contact - (unmcrsa@unmc.edu)
University of New Mexico Cancer Center Albuquerque, New Mexico Site Public Contact - (HSC-ClinicalTrialInfo@salud.unm.edu)
University of Oklahoma Health Sciences Center Oklahoma City, Oklahoma Site Public Contact - (ou-clinical-trials@ouhsc.edu)
University of Rochester Rochester, New York
University of Texas at Austin Austin, Texas
University of Virginia Cancer Center Charlottesville, Virginia Site Public Contact - (uvacancertrials@hscmail.mcc.virginia.edu)
University of Wisconsin Carbone Cancer Center - Eastpark Medical Center Madison, Wisconsin Site Public Contact - (clinicaltrials@cancer.wisc.edu)
University of Wisconsin Carbone Cancer Center - University Hospital Madison, Wisconsin Site Public Contact - (clinicaltrials@cancer.wisc.edu)
Upper Valley Medical Center Troy, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
VCU Massey Cancer Center at Stony Point Richmond, Virginia Site Public Contact - (ctoclinops@vcu.edu)
VCU Massey Comprehensive Cancer Center Richmond, Virginia Site Public Contact - (CTOclinops@vcu.edu)
Virtua Samson Cancer Center Moorestown, New Jersey
Virtua Voorhees Voorhees Township, New Jersey
Wake Forest University Health Sciences Winston-Salem, North Carolina
Walter Reed National Military Medical Center Bethesda, Maryland
Washington University School of Medicine St Louis, Missouri Site Public Contact - (info@siteman.wustl.edu)
Wayne State University/Karmanos Cancer Institute Detroit, Michigan
Weisberg Cancer Treatment Center Farmington Hills, Michigan
West Jefferson Medical Center Marrero, Louisiana Site Public Contact - (emede1@lsuhsc.edu)
West Michigan Cancer Center Kalamazoo, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
West Penn Hospital Pittsburgh, Pennsylvania
West Virginia University Charleston Division Charleston, West Virginia
West Virginia University Healthcare Morgantown, West Virginia Site Public Contact - (cancertrialsinfo@hsc.wvu.edu)
Wexford Health and Wellness Pavilion Wexford, Pennsylvania
William E Kahlert Regional Cancer Center/Sinai Hospital Westminster, Maryland
Wilmot Cancer Institute at Webster Webster, New York Site Public Contact - (WCICTOresearch@urmc.rochester.edu)
Women and Infants Hospital Providence, Rhode Island
Women's Cancer Care Associates LLC Albany, New York Site Public Contact - (jbarlin@womenscancercareassociates.com)
Women's Cancer Center of Nevada Las Vegas, Nevada
Women's Diagnostic Center - Munster Munster, Indiana Site Public Contact - (mnicholson@comhs.org)
Yale University New Haven, Connecticut Site Public Contact - (canceranswers@yale.edu)
Yale-New Haven Hospital North Haven Medical Center North Haven, Connecticut Site Public Contact - (canceranswers@yale.edu)

A Study of Mavacamten in Non-Obstructive Hypertrophic Cardiomyopathy (ODYSSEY_HCM)

BMS Study Connect Contact Center www.BMSStudyConnect.com - Clinical.Trials@bms.com

NCT05582395
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Inclusion Criteria:

• Diagnosis of HCM consistent with current American College of Cardiology Foundation/American Heart Association and European Society of Cardiology guidelines: unexplained left-ventricular hypertrophy with non-dilated ventricular chambers in the absence of other cardiac or systemic disease which can produce the required magnitude of hypertrophy of a maximal left ventricular (LV) wall thickness ≥ 15 millimeters (mm) (or ≥ 13 mm with positive family history of hypertrophic cardiomyopathy [HCM]) as determined by core laboratory interpretation
• Peak left ventricular outflow tract (LVOT) pressure gradient < 30 millimeters mercury (mm Hg) at rest and < 50 mm Hg with provocation (Valsalva maneuver and stress echocardiography)
• New York Heart Association (NYHA) Class II or III
Exclusion Criteria:

• Known infiltrative or storage disorder causing cardiac hypertrophy that mimics non-obstructive hypertrophic cardiomyopathy (nHCM) such as Fabry disease, amyloidosis, or Noonan syndrome with LV hypertrophy
• History of unexplained syncope within 6 months prior to screening
• History of sustained ventricular tachyarrhythmia (> 30 seconds) within 6 months prior to screening Additional inclusion and exclusion criteria apply.
Drug: Mavacamten, Other: Placebo
Cardiomyopathy, Hypertrophic
Mavacamten, non-obstructive HCM, non-obstructive hypertrophic cardiomyopathy (nHCM)
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Show 197 locations

Study Locations

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Location Contacts
Baylor Scott and White Research Institute Dallas, Texas Robert Gottlieb, Site 0089
Carolinas HealthCare System Charlotte, North Carolina John Symanski, Site 0094
Cedars-Sinai Heart Institute Los Angeles, California Florian Rader, Site 0010
Cleveland Clinic Ohio - 9500 Euclid Ave Cleveland, Ohio Milind Desai, Site 0083
Duke University Health System Durham, North Carolina Andrew Wang, Site 0065
Emory University Hospital Atlanta, Georgia Ozlem Bilen, Site 0092
Henry Ford Hospital Detroit, Michigan Karthikeyan Ananthasubramaniam, Site 0064
Indiana University School of Medicine-Indianapolis Indianapolis, Indiana Roopa Rao, Site 0424
Johns Hopkins University Baltimore, Maryland Jose Madrazo, Site 0127
Lancaster General Hospital Lancaster, Pennsylvania Robert Donovan, Site 0444
Local Institution - 0001 Lenexa, Kansas Site 0001
Local Institution - 0003 Oakland, California Site 0003
Local Institution - 0004 ABB, Buenos Aires F.D. Site 0004
Local Institution - 0005 Santiago, Santiago Metropolitan Site 0005
Local Institution - 0006 Santiago, Santiago Metropolitan Site 0006
Local Institution - 0008 Ciudad Autónoma de Buenos Aires, Buenos Aires Site 0008
Local Institution - 0009 Pittsburgh, Pennsylvania Site 0009
Local Institution - 0011 Paris, Site 0011
Local Institution - 0012 Marseille, Site 0012
Local Institution - 0013 Clearwater, Florida Site 0013
Local Institution - 0014 Strasbourg, Alsace Site 0014
Local Institution - 0015 Paris, Site 0015
Local Institution - 0016 Lima, LIM Site 0016
Local Institution - 0017 Toulouse, Haute-Garonne Site 0017
Local Institution - 0018 La Tronche, Isère Site 0018
Local Institution - 0019 Villejuif, Val-de-Marne Site 0019
Local Institution - 0021 La Jolla, California Site 0021
Local Institution - 0022 Yvoir, Namur Site 0022
Local Institution - 0023 Ghent, Oost-Vlaanderen Site 0023
Local Institution - 0024 Sint-Niklaas, Oost-Vlaanderen Site 0024
Local Institution - 0025 Houston, Texas Site 0025
Local Institution - 0026 New York, New York Site 0026
Local Institution - 0027 New Orleans, Louisiana Site 0027
Local Institution - 0028 Ravenna, Emilia-Romagna Site 0028
Local Institution - 0030 Beijing, Beijing Municipality Site 0030
Local Institution - 0031 Orbassano, Piedmont Site 0031
Local Institution - 0032 Milan, Site 0032
Local Institution - 0033 Wenzhou, Zhejiang Site 0033
Local Institution - 0034 Naples, Site 0034
Local Institution - 0035 New York, New York Site 0035
Local Institution - 0037 Portland, Oregon Site 0037
Local Institution - 0038 Portland, Oregon Site 0038
Local Institution - 0039 Zuerich, Site 0039
Local Institution - 0040 Evanston, Illinois Site 0040
Local Institution - 0041 St.Gallen, HE Site 0041
Local Institution - 0042 Seoul, Seoul-teukbyeolsi [Seoul] Site 0042
Local Institution - 0043 Goyang-si, Kyǒnggi-do Site 0043
Local Institution - 0044 Seongnam, Kyǒnggi-do Site 0044
Local Institution - 0045 Seoul, Seoul-teukbyeolsi [Seoul] Site 0045
Local Institution - 0046 Suwon, Kyǒnggi-do Site 0046
Local Institution - 0048 Shenyang, Liaoning Site 0048
Local Institution - 0049 Kansas City, Kansas Site 0049
Local Institution - 0050 Grand Rapids, Michigan Site 0050
Local Institution - 0051 Sevilla, MZ Site 0051
Local Institution - 0052 Mainz, Rheinland-Pfalz Site 0052
Local Institution - 0053 Burlington, Ontario Site 0053
Local Institution - 0054 Athens, Attikí Site 0054
Local Institution - 0055 Lima, Site 0055
Local Institution - 0056 Thessaloniki, Kentrikí Makedonía Site 0056
Local Institution - 0057 Hannover, Site 0057
Local Institution - 0059 Los Angeles, California Site 0059
Local Institution - 0060 Chaïdári, Attikí Site 0060
Local Institution - 0061 London, Kensington and Chelsea Site 0061
Local Institution - 0062 Thessaloniki, Thessaloníki Site 0062
Local Institution - 0063 Brno, JM Site 0063
Local Institution - 0066 Massillon, Ohio Site 0066
Local Institution - 0067 Hackensack, New Jersey Site 0067
Local Institution - 0069 Bengaluru, Karnataka Site 0069
Local Institution - 0071 Mumbai, Maharashtra Site 0071
Local Institution - 0072 Gurugram, Haryana Site 0072
Local Institution - 0073 Ahmedabad, Gujarat Site 0073
Local Institution - 0074 Montpellier, Languedoc-Roussillon Site 0074
Local Institution - 0075 Chengdu, Sichuan Site 0075
Local Institution - 0076 Villejuif, Val-de-Marne Site 0076
Local Institution - 0077 Mumbai, Maharashtra Site 0077
Local Institution - 0078 Howrah, West Bengal Site 0078
Local Institution - 0080 Iowa City, Iowa Site 0080
Local Institution - 0085 Gainesville, Florida Site 0085
Local Institution - 0086 Linz, Site 0086
Local Institution - 0087 Richmond, Virginia Site 0087
Local Institution - 0090 Bordeaux, Aquitaine Site 0090
Local Institution - 0091 Victoria, British Columbia Site 0091
Local Institution - 0093 Salamanca, Site 0093
Local Institution - 0119 Iași, Site 0119
Local Institution - 0160 Budapest, Pest Site 0160
Local Institution - 0168 Kashiwa, Chiba Site 0168
Local Institution - 0171 Portland, Oregon Site 0171
Local Institution - 0174 Chapel Hill, North Carolina Site 0174
Local Institution - 0188 Brno, Jihomoravský Kraj Site 0188
Local Institution - 0203 Tōon, Ehime Site 0203
Local Institution - 0208 Chemnitz, Saxony Site 0208
Local Institution - 0213 Cologne, North Rhine-Westphalia Site 0213
Local Institution - 0217 Sapporo, Hokkaido Site 0217
Local Institution - 0221 Boulogne-Billancourt, Hauts-de-Seine Site 0221
Local Institution - 0224 Oaxaca City, Oaxaca Site 0224
Local Institution - 0237 San Juan, Site 0237
Local Institution - 0253 Melbourne, Victoria Site 0253
Local Institution - 0258 Taiyuan, Shanxi Site 0258
Local Institution - 0273 Ahmedabad, Gujarat Site 0273
Local Institution - 0289 Tianjin, Tianjin Municipality Site 0289
Local Institution - 0299 Heidelberg,VIC, Victoria Site 0299
Local Institution - 0314 Donostia / San Sebastian, Gipuzkoa Site 0314
Local Institution - 0319 Fukuoka, Site 0319
Local Institution - 0330 Katowice, Silesian Voivodeship Site 0330
Local Institution - 0338 Amsterdam, Site 0338
Local Institution - 0357 Gosford, New South Wales Site 0357
Local Institution - 0369 New York, New York Site 0369
Local Institution - 0370 Essen, Site 0370
Local Institution - 0373 Firenze, Site 0373
Local Institution - 0381 London, LND Site 0381
Local Institution - 0403 Mersin, Site 0403
Local Institution - 0404 Ulm, Site 0404
Local Institution - 0407 Ahmedabad, Gujarat Site 0407
Local Institution - 0411 Mexico City, Mexico City Site 0411
Local Institution - 0412 A Coruña, A Coruña [La Coruña] Site 0412
Local Institution - 0413 Guadalajara, Site 0413
Local Institution - 0414 Nagpur, MH Site 0414
Local Institution - 0415 Margate, Florida Site 0415
Local Institution - 0416 Riyadh, Site 0416
Local Institution - 0417 Szeged, Site 0417
Local Institution - 0418 São Paulo, SAO Paulo Site 0418
Local Institution - 0419 Haifa, Site 0419
Local Institution - 0420 Sarıçam, Adana Site 0420
Local Institution - 0421 Buenos Aires, Buenos Aires F.D. Site 0421
Local Institution - 0422 Ankara, Site 0422
Local Institution - 0423 Kitakyushu-shi, Fukuoka Site 0423
Local Institution - 0425 Belo Horizonte, Minas Gerais Site 0425
Local Institution - 0427 Singapore, Central Singapore Site 0427
Local Institution - 0428 Chiang Mai, Site 0428
Local Institution - 0429 Srinagar, Jammu and Kashmir Site 0429
Local Institution - 0430 Kochi, Kerala Site 0430
Local Institution - 0433 New Delhi, Delhi Site 0433
Local Institution - 0434 Bangkok, Bangkok Site 0434
Local Institution - 0436 Edgewood, Kentucky Site 0436
Local Institution - 0437 Kansas City, Missouri Site 0437
Local Institution - 0438 Jeddah, Site 0438
Local Institution - 0439 Dammam, Eastern Province Site 0439
Local Institution - 0440 Osijek, Site 0440
Local Institution - 0441 Deagu, Taegu-Kwangyǒkshi Site 0441
Local Institution - 0442 Daegu, Taegu-Kwangyǒkshi Site 0442
Local Institution - 0443 Box Hill, Victoria Site 0443
Local Institution - 0445 Riyadh, Riyadh Region Site 0445
Local Institution - 0446 Buenos Aires, Site 0446
Local Institution - 0447 Santiago, Site 0447
Local Institution - 0448 Guadalajara, Jalisco Site 0448
Local Institution - 0450 Tulsa, Oklahoma Site 0450
Local Institution - 0451 Keçiören/Ankara, Site 0451
Local Institution - 0452 Atlanta, Georgia Site 0452
Local Institution - 0453 Lembah Pantai, Kuala Lumpur Site 0453
Local Institution - 0454 Pilea Chortiatis, Thessaloniki Site 0454
Local Institution - 0456 Seongnam, Kyǒnggi-do Site 0456
Local Institution - 0457 Nagpur, Maharashtra Site 0457
Local Institution - 0459 Santiago, Santiago Metropolitan Site 0459
Local Institution - 0460 Graz, Styria Site 0460
Local Institution - 0462 Auckland, Site 0462
Local Institution - 0463 Hermosillo, Sonora Site 0463
Local Institution - 0466 Pittsburgh, Pennsylvania Site 0466
Local Institution - 0467 Darlinghurst, New South Wales Site 0467
Local Institution - 0470 Santa Cruz de Tenerife, Site 0470
Local Institution - 0471 Coimbatore, Tamil Nadu Site 0471
Local Institution - 0472 London, Middlesex Site 0472
Local Institution - 0473 Graz, Styria Site 0473
Local Institution - 0475 Eiheiji-cho,Yoshida-gun, Fukui Site 0475
Local Institution - 0476 Engenho Velho da Federação, Salvador Site 0476
Local Institution - 0477 Lucknow, Uttar Pradesh Site 0477
Local Institution - 0480 Hackensack, New Jersey Site 0480
Massachusetts General Hospital Boston, Massachusetts Albree Tower-Rader, Site 0479
Mayo Clinic - PPDS Rochester, Minnesota Jeffrey B. Geske, Site 0431
Mayo Clinic Arizona - PPDS Phoenix, Arizona Said Alsidawi, Site 0458
Medical University of South Carolina - PPDS Charleston, South Carolina Jessica Atkins, Site 0058
North Shore University Hospital-300 Community Dr Manhasset, New York Ronald Wharton, Site 0449
Oregon Health and Science University Portland, Oregon Ahmad Masri, Site0084
Penn State Health Milton S. Hershey Medical Center Hershey, Pennsylvania Eric Popjes, Site 0047
Spectrum Health Grand Rapids, Michigan David Fermin, Site 0455
St. Luke's University Health Network Bethlehem, Pennsylvania Jamshid Shirani, Site 0020
Stanford University Palo Alto, California Matthew Wheeler, Site 0079
Stern Cardiovascular Foundation Inc Southaven, Mississippi Frank McGrew, Site 0207
Stony Brook Heart Institute Stony Brook, New York Michael Gavalas, Site 0007
UCSF School of Medicine San Francisco, California Theodore Abraham, Site 0406
University of Alabama at Birmingham: The Kirklin Clinic Birmingham, Alabama Jose Tallaj, Site 0082
University of California San Diego San Diego, California Eric Adler, Site 0409
University of Florida Gainesville, Florida Mohammad Al-Ani, Site 0468
University of Iowa Hospitals and Clinics Iowa City, Iowa Ernesto Ruiz Duque, Site 0070
University of Kansas Medical Center Kansas City, Kansas Loren Berenbom, Site 0410
University of Michigan Comprehensive Cancer Center UMCCC-Gastrointestinal Cancer Clinic Ann Arbor, Michigan Sara Saberi, Site 0464
University of Nebraska Medical Center Omaha, Nebraska Douglas Stoller, Site 0435
University of Pennsylvania Philadelphia, Pennsylvania Anjali Owens, Site 0263
University of Pittsburgh Medical Center Pittsburgh, Pennsylvania Timothy Wang, Site 0081
University of Texam Houston Medical School Houston, Texas Ali Marian, Site0002
University of Texas Southwestern Medical Center Dallas, Texas James MacNamara, Site 0365
University of Utah - PPDS Salt Lake City, Utah Omar Wever-Pinzon, Site 0402
University of Virginia Health System Charlottesville, Virginia Christopher Kramer, Site 0478
University of Washington Medical Center Seattle, Washington David Owens, Site 0342
Usf Health South Tampa Center For Advanced Healthcare Tampa, Florida Thomas McDonald, Site 0281
Virginia Commonwealth University Medical Center Richmond, Virginia Mohammed Makkiya, Site 0095
Washington University School of Medicine St Louis, Missouri Richard Bach, Site 0461
Westchester Medical Center Valhalla, New York Srihari Naidu, Site 0426

Neutrophil and Monocyte Deactivation Via the SeLective CytopheretIc Device - A Randomized Clinical Trial in Acute Kidney Injury (NEUTRALIZE-AKI)

Mohamed Zidan, MD - mzidan@seastarmed.com

NCT05758077
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Inclusion Criteria:
* Admitted to an ICU requiring CKRT:
• Must have AKI stage 2 or greater at the time of CKRT initiation.
• Must have been on CKRT for at least 12 hours but no greater than 48 hours at the time of enrollment. * At least 18 years of age but not older than 80 at the time of enrollment. * One additional life-threatening organ dysfunction present. * Acceptable vascular access for CKRT to include adequate lumen size and length of catheters. * Initial (non-binding) commitment to maintaining current level of care for at least 96 hours. * C-Reactive Protein \>3.5 mg/dl.
Exclusion Criteria:
* Not expected to survive next 24 hours. * Anticipated transition to comfort measures or hospice in next 4 days. * Terminal condition whereby the patient is not expected to survive 28 days or any condition in which therapy is regarded as futile by the PI. * Advanced malignancy which is actively being treated or may be treated with palliative chemotherapy or radiation. * ICU hospitalization \> 14 days during this hospital admission (to include days spent at ICU of an outside hospital) at the time of screening. * Active COVID-19 infection with a primary admission diagnosis of COVID-19. * Chronic use of ventricular assist devices. * ESRD requiring chronic kidney replacement therapy. * History of CKD (greater than Stage 3). * AKI stage 0 or stage 1 at the time of CKRT initiation. * Non-ATN AKI diagnosis. We intend on relying on local nephrology subspecialty expertise to reasonably exclude non-ATN diagnoses based on clinical suspicions combined with prespecified objective criteria. If there is a reasonable suspicion that the subject has non-ATN AKI based on this, they will be excluded from the trial. * Acute coronary syndromes, acute stroke, or acute major vascular compromise requiring medical or surgical interventions within 48 hours of randomization. * Active hemorrhage requiring blood transfusions at the time of screening. * Acute on Chronic Liver Failure. * Suspicion of hepato-renal syndrome. * Presence of any solid organ transplant at any time prior to admission. * Severe burns with a modified Baux score \> 100 (%TBSA+Age+17 for Inhalation Injury). * Bone marrow transplant within the last year. * Chronic immunosuppression with an average of \>20 mg/day of prednisone or other steroid sparing immunosuppressants for the past 30 days prior to hospital admission. * Individuals who have a history of primary or secondary immune disorders including, but not limited to, HIV or AIDS. * Dry weight of \>150kg. * Platelet count \<15,000/mm3. * Patient is a prisoner or member of a vulnerable population. * Patient is pregnant or breast feeding. * Concurrent enrollment in another interventional clinical trial for an investigational drug or device. * Need for plasmapheresis.
DEVICE: Selective Cytopheretic Device, OTHER: Standard of Care
Acute Kidney Injury
continuous kidney replacement therapy, continuous renal replacement therapy, acute kidney injury, organ failure, inflammation, dialysis, acute tubular necrosis
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Study Locations

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Location Contacts
AdventHealth Orlando Apopka, Florida
Brooke Army Medical Center Houston, Texas
Central Arkansas Veterans Healthcare Little Rock, Arkansas
Cleveland Clinic Cleveland, Ohio
Geisinger Wyoming Valley Medical Center Wilkes-Barre, Pennsylvania
Henry Ford Medical Center Sterling Heights, Michigan
JMS Burn Center Augusta, Georgia
Mayo Clinic Rochester, Minnesota
Medical University of South Carolina Charleston, South Carolina
Methodist Hospital Saint Louis Park, Minnesota
Methodist Hospital Metropolitan San Antonio, Texas
Nazareth Hospital Philadelphia, Pennsylvania
Ochsner LSU Health Academic Medical Center Shreveport, Louisiana
Orlando Regional Medical Center Orlando, Florida
Ronald Reagan UCLA Medical Center Los Angeles, California
Saint Mary Medical Center Hobart, Indiana
Samaritan Health Corvallis, Oregon
Sentara Health Norfolk, Virginia
St Luke's University Hospital Bethlehem, Pennsylvania
Stanford University Palo Alto, California
UNLV Health Las Vegas, Nevada
United States Army Institute of Surgical Research JBSA Fort Sam Houston, Texas
University of Alabama Birmingham Hospital Birmingham, Alabama
University of Cincinnati Cincinnati, Ohio
University of Colorado Hospital Anschutz Medical Campus Aurora, Colorado
University of Iowa Hospital Iowa City, Iowa
University of Kentucky Healthcare Lexington, Kentucky
University of Michigan Ann Arbor, Michigan
University of North Carolina Chapel Hill, North Carolina
University of Texas Health San Antonio San Antonio, Texas
University of Texas Southwestern Medical Center Dallas, Texas
Unversity of Rochester Rochester, New York
Virginia Commonwealth University Richmond, Virginia

Pediatric Obesity Weight Evaluation Registry (POWER) Study (POWER)

Shelley Kirk, PhD, RD, LD - Shelley.Kirk@cchmc.org

NCT02121132
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Inclusion Criteria:

• age 18 years or younger
• overweight or obese patient
• initial medical evaluation in a pediatric weight management program between March 1, 2014-April 30, 2020.
Exclusion Criteria:

• no exclusion criteria
Overweight, Obesity
Overweight, Obesity
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Show 38 locations

Study Locations

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Location Contacts
AdventHealth Orlando, Florida Mary Beth Vance - (mary.vance@adventhealth.com)
Advocate Children's Hospital Park Ridge, Illinois Susan Panek - (susan.panek@aah.org)
Ann & Robert H. Lurie Children's Hospital of Chicago Chicago, Illinois
Arkansas Children's Hospital Little Rock, Arkansas
Children's Healthcare of Atlanta Atlanta, Georgia
Children's Hospital Los Angeles Los Angeles, California
Children's Hospital and Medical Center Omaha Omaha, Nebraska Leslie Turner - (lturner@childrensomaha.org)
Children's Hospital of San Antonio San Antonio, Texas
Children's Medical Center at UT Southwestern Dallas, Texas
Children's Mercy Hospital Kansas City, Missouri
Cincinnati Children's Hospital Medical Center Cincinnati, Ohio
Cleveland Clinic Cleveland, Ohio Roy Kim - (kimr@ccf.org)
Connecticut Children's Medical Center Hartford, Connecticut
Cook Children's Medical Center Fort Worth, Texas
Dell Children's Medical Center Austin, Texas
Duke Children's Hospital & Health Center Durham, North Carolina
Eastern Maine Medical Center Bangor, Maine
Fit Kids of Arizona at Northern Arizona Healthcare Cottonwood, Arizona Dirk de Heer - (dirk.deheer@nau.edu)
Helen DeVos Children's Hospital Grand Rapids, Michigan
Maine Medical Center - Barbara Bush Children's Hospital Portland, Maine
Marshfield Clinic Weston, Wisconsin
Mayo Clinic in Minnesota Rochester, Minnesota
OSF Saint Francis Medical Center Peoria, Illinois
Our Lady of The Lake Baton Rouge, Louisiana Micah Klumpp - (micah.klumpp@fmolhs.org)
Penn State Hershey Children's Hospital Hershey, Pennsylvania
Riley Children's Hospital - IU Health Indianapolis, Indiana Emily Ragozzino - (emragozz@iu.edu)
Seattle Children's Hospital Seattle, Washington
St. Luke's Children's Hospital Boise, Idaho
The Medical University of South Carolina Charleston, South Carolina Christine San Giovanni - (sangiova@musc.edu)
UCSF Benioff Children's Hospital Oakland Oakland, California
University of California Los Angeles Los Angeles, California Jennifer Yee - (jyee@lundquist.org)
University of Florida Health Science Center Jacksonville, Florida
University of Michigan C.S. Mott Children's Hospital Ann Arbor, Michigan
University of Minnesota Amplatz Children's Hospital Minneapolis, Minnesota
University of Mississippi Medical Center Jackson, Mississippi
University of New Mexico Children's Hospital Albuquerque, New Mexico
University of Oklahoma Health Sciences Center Oklahoma City, Oklahoma
VCU Health Richmond, Virginia Sarah Farthing - (sarah.malone@vcuhealth.org)

Pharmacokinetics, Safety and Efficacy of the Selumetinib Granule Formulation in Children Aged ≥1 to <7 Years With NF1-related Symptomatic, Inoperable PN (SPRINKLE)

AstraZeneca Clinical Study Information Center - information.center@astrazeneca.com

NCT05309668
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Inclusion Criteria:

• Male and female participants aged ≥ 1 to < 7 years of age at the time their legally authorised representative (parent or guardian) signs the informed consent.
• All study participants must be diagnosed with NF1 with symptomatic inoperable PN as defined in protocol.
• Participants must have at least one measurable PN, defined as a PN of at least 3 cm measured in one dimension, which can be seen on at least 3 imaging slices and have a reasonably well-defined contour. Participants who have undergone surgery for resection of a PN are eligible provided the PN was incompletely resected and is measurable. The target PN will be defined as the clinically most relevant PN, which is symptomatic, inoperable and measurable by volumetric MRI analysis.
• Performance status: Participants must have a Lansky performance of ≥ 70 except in participants who are wheelchair bound or have limited mobility secondary to a need for mechanical breathing support (such as an airway PN requiring tracheostomy or continuous positive airway pressure) who must have a Lansky performance of ≥ 40.
• Participants must have a BSA ≥ 0.4 and ≤ 1.09 m2 at study entry (date of ICF signature).
• Mandatory provision of consent for the study signed and dated by a participant's legally authorised representative (parent or guardian) along with the paediatric assent form, if applicable.
Exclusion Criteria:

• Participants with confirmed or suspected malignant glioma or MPNST. Participants with low grade glioma (including optic glioma) not requiring systemic therapy are permitted.
• History of malignancy except for malignancy treatment with curative intent with no known active disease ≥ 2 years before the first dose of study intervention and of low potential risk of recurrence.
• Refractory nausea and vomiting, chronic gastrointestinal disease, inability to swallow the formulated product, or previous significant bowel resection that would preclude adequate absorption, distribution, metabolism, or excretion of selumetinib.
• A life-threatening illness, medical condition, organ system dysfunction or laboratory finding which, in the Investigator's opinion, could compromise the participant's safety, interfere with the absorption or metabolism of selumetinib, or put the study outcomes at undue risk.
• Participants with clinically significant cardiovascular disease as defined in the protocol.
• Liver function tests: Bilirubin > 1.5 × the ULN for age with the exception of those with Gilbert syndrome (≥ 3 × ULN) or AST/ALT > 2 × ULN.
• Renal Function: Creatinine clearance or radioisotope glomerular filtration rate < 60 mL/min/1.73 m2 or Serum creatinine > 0.8 mg/dL (for participants aged ≥ 1 to < 4 years) or > 1.0 mg/dL (for participants aged ≥ 4 years).
• Participants with ophthalmological findings/condition as listed in the protocol.
• Have any unresolved chronic toxicity with CTCAE Grade ≥ 2 which are associated with previous therapy for NF1-PN (except hair changes such as alopecia or hair lightening)
• Participants who have previously been treated with a MEKi (including selumetinib) and have had disease progression, or due to toxicity have either discontinued treatment and/or required a dose reduction.
• Have inadequate haematological function defined as: An absolute neutrophil count < 1500/μL or Haemoglobin < 9g/dL or Platelets <100,000/μL or Have had a transfusion (of red cells or other blood derived products) within the 28 days prior to study entry (date of ICF signature).
• Have received or are receiving an IMP or other systemic NF1-PN target treatment (including MEKi) within 4 weeks prior to the first dose of study intervention, or within a period during which the IMP or systemic PN target treatment has not been cleared from the body (eg, a period of 5 'half-lives'), whichever is longer.
• Has received radiotherapy in the 6 weeks prior to start of study intervention or any prior radiotherapy directed at the target or non-target PN.
• Receiving herbal supplements or medications known to be strong or moderate inhibitors of the CYP3A4 and CYP2C19 enzymes or inducers of the CYP3A4 enzyme unless such products can be safely discontinued at least 14 days or 5 half-lives (whichever is longer) before the first dose of study medication.
• Inability to undergo MRI and/or contraindication for MRI examinations. Prosthesis or orthopaedic or dental braces that would interfere with volumetric analysis of target PN on MRI.
Drug: Selumetinib granule formulation, Drug: Selumetinib capsule formulation
Neurofibromatosis Type 1
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Study Locations

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Location Contacts
Children's Hospital of Philadelphia Philadelphia, Pennsylvania
Children's Hospital of Richmond at VCU Richmond, Virginia
Childrens Hospital Medical Center - Akron Akron, Ohio
Erasmus University Medical Center Rotterdam Rotterdam,
Fondazione I.R.C.C.S. Istituto Neurologico Carlo Besta Milano,
Hospital Sant Joan de Deu Barcelona,
Nagoya University Hospital Nagoya,
National Center for Child Health and Development Tokyo, Setagaya-ku,
Oita University Hospital Yufu, Oita Prefecture
Ospedale Infantile Regina Margherita Torino, Turin
Ospedale Pediatrico Bambino Gesu' di Roma Roma,
Phoenix Children's Hospital Phoenix, Arizona
Research Site Moscow,
Research Site Moscow,
Research Site Moscow,
Research Site Moscow,
Research Site Moscow,
Research Site Moscow,
Texas Children's Hospital Houston, Texas
University of Indiana (IU) Health - Riley Hospital for Children Indianapolis, Indiana

Remote Monitoring and Management of Chemotherapy Induced Peripheral Neuropathy (REMOTE-CIPN)

Noah A Kolb, MD - noah.kolb@uvmhealth.org

NCT04763356
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Inclusion Criteria:
In order to be eligible to participate in this study, an individual must meet all of the following criteria:
• Age ≥ 18.
• Completion of taxane, platinum, vinca alkaloid-based chemotherapy, bortezomib, thalidomide, lenalidomide, ixazomib, or brentuximab vedotin for cancer in the last 540 days, or ongoing maintenance therapy with bortezomib, thalidomide, lenalidomide or ixazomib for \> 90 days or ongoing survival, palliative or equivalent therapy with any of the above listed drugs for \>90 days.
• Development of CIPN during or within 3 months of the most recently completed chemotherapy or previous neurotoxic chemotherapy for the same malignancy. For patients on ongoing maintenance therapy: Development of CIPN during current neurotoxic chemotherapy with bortezomib, thalidomide, lenalidomide, ixazomib brentuximab vendotin or vincristine. CIPN diagnosis will be based on clinical diagnosis and the Toronto Criteria for Probable Distal Symmetric Polyneuropathy including the upper and lower extremities. The Toronto Criteria for Probable Distal Symmetric Polyneuropathy is defined as a combination of symptoms and signs of neuropathy including:
• At least 1 (one) of the following neuropathic symptoms: "asleep numbness", prickling or stabbing, burning or aching pain AND
• At least 1 (one) of the following: decreased distal sensation, or unequivocally decreased or absent ankle reflexes. (59) Clinical Diagnosis: a. Confirmation of CIPN diagnosis by CIPN expert (investigator/co-infestigator based on chart review +/- inperson/virtual interview with examination).
• Presence of at least one positive neuropathic sensory symptom on the NTSS-6 ranked as moderate or severe on the day of screening or in the preceding week based on recall.
• The ability to speak/ read sufficient English to be able to communicate with study NP over the phone, utilize the App, website and phone tree (all of which are only available in English).
Exclusion Criteria:
An individual who meets any of the following criteria will be excluded from participation in this study:
• Expected treatment with another neurotoxic chemotherapy within the 13 week overall study duration (For example, platinum, taxane, vinca alkaloid, thalidomide, brentuximab vedotin or related drug, or arsenic trioxide. This exclusion does not apply to continuation of treatment for patients on maintenance therapy as described in the inclusion criteria).
• Presence of a neurological problem that would confound CIPN assessment (lumbar or cervical radiculopathy, or pre-existing neuropathy from another cause such as diabetes).
• Currently receiving treatment at a pain clinic specifically for CIPN pain.
• Concurrent participation in a different CIPN or pain treatment trial.
• For women of childbearing potential: Current pregnancy
• For women of childbearing potential: Unwillingness to use and acceptable form of birth control for the duration of the study. Acceptable forms of birth control include long acting implantable contraception (ie IUDs, Nexplanon), Oral contraception pills, contraception injections, or strict abstinence if it is part of the subject's current lifestyle.
OTHER: Symptom Care at Home with NP follow up
Chemotherapy-induced Peripheral Neuropathy
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Study Locations

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Location Contacts
University of Utah Salt Lake City, Utah Samantha Stebleton - (samantha.stebleton@nurs.utah.edu) Christina Echeverria, MA - (christina.echeverria@nurs.utah.edu)
University of Vermont Burlington, Vermont Hannah Taylor, BA - (hannah.taylor@uvmhealth.org) Mary Healey, BA - (mary.healey@uvmhealth.org)
Virginia Commonwealth University Massey Cancer Center Richmond, Virginia Melanie Crabtree - (crabtreemb@vcu.edu) Tyler Phillips - (phillipst5@vcu.edu)

Exploring the Familial Reach of Adolescent Obesity Treatment

Sarah M Farthing, MS - sarah.malone@vcuhealth.org

NCT05780970
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Inclusion Criteria:

• Untreated children: must be between 8-17 years of age and primarily living in the same household as the TEENS+ participants.
• Untreated caregiver: must be 18 years of age or older and primarily living in the same household as the TEENS+ participants.
• Treated caregivers: must have another individual in the household that meets the eligbility for an untreated child or untreated caregiver.
Exclusion Criteria:

• temporarily (<1yr) living in the home
• children with a BMI<5th%ile or caregivers with a BMI<18.5 kg/m2
• non-English speaking
• medical condition(s) that may be associated with unintentional weight change or significant disruption to eating behaviors (e.g., hypothalamic injury, Prader-Willi, G-tube placement, or malignancy
• clinically significant eating disorder (e.g., anorexia nervosa or bulimia nervosa)
• following a medically-supervised/prescribed diet
• psychiatric, cognitive, physical or developmental conditions that would impair the individual's ability to complete assessments.
Other: No intervention
Pediatric Obesity
Pediatric Obesity, Lifestyle Intervention, Family-Level Change, Family-based Intervention
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Study Locations

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Location Contacts
Children's Hospital of Richmond at VCU Healthy Lifestyles Center Henrico, Virginia Sarah M Farthing, MS - (sarah.malone@vcuhealth.org) Melanie K Bean, Ph.D. - (melanie.bean@vcuhealth.org)

Colon Adjuvant Chemotherapy Based on Evaluation of Residual Disease (CIRCULATE-US)

Judy Langer - langerj@nrgoncology.org

NCT05174169
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Inclusion Criteria:
The patient must have an ECOG performance status of 0 or 1. Patients must have histologically/pathologically confirmed Stage IIB, IIC, or Stage III colon adenocarcinoma with R0 resection according to AJCC 8th edition criteria. No radiographic evidence of overt metastatic disease within 45 days prior to Step 1/Study entry (CT with IV contrast or MRI imaging is acceptable and must include chest, abdomen, and pelvis). The distal extent of the tumor must be greater than or equal to 12 cm from the anal verge on colonoscopy or above the peritoneal reflection as documented during surgery or on pathology specimen (i.e., excluding rectal adenocarcinomas warranting treatment with chemoradiation). The patient must have had an en bloc complete gross resection of tumor (curative resection). Patients who have had a two-stage surgical procedure, to first provide a decompressive colostomy and then in a later procedure to have the definitive surgical resection, are eligible. The resected tumor specimen and a blood specimen from patients with Stage IIB, IIC, or Stage III colon cancer must have central testing for ctDNA using the Signatera™ assay by Natera (after Step 1/Study entry and before Step2/Randomization). Patient must have sufficient tissue to meet protocol requirements. This blood specimen for the Signatera assay must be collected after surgery (and recommended at least 14 days post surgery). Tumor must be documented as microsatellite stable or have intact mismatch repair proteins through CLIA-approved laboratory testing. Patients whose tumors are MSI-H or dMMR are excluded. The treating investigator must deem the patient a candidate for all potential agents used in this trial (5FU, LV, oxaliplatin and irinotecan). The interval between surgery (post-operative Day 7) and Step 1/Study entry must be no more than 60 days. NOTE: Step 1/Study Entry may occur as early as post operative Day 7, but it cannot occur beyond 60 days from the actual date of the patient's surgery. Availability and provision of adequate surgical tumor tissue for molecular diagnostics and confirmatory profiling. Adequate hematologic function within 28 days before Step 1/Study entry defined as follows: * Absolute neutrophil count (ANC) must be greater than or equal to 1500/mm3; * Participants with benign ethnic neutropenia (BEN): ANC less than 1300 mm3 are eligible. * BEN (also known as constitutional neutropenia) is an inherited cause of mild or moderate neutropenia that is not associated with any increased risk for infections or other clinical manifestations. BEN is referred to as ethnic neutropenia because of its increased prevalence in people of African descent and other specific ethnic groups. * Platelet count must be greater than or equal to 100,000/mm3; and * Hemoglobin must be greater than or equal to 9 g/dL. Adequate hepatic function within 28 days before Step 1/Study entry defined as follows: * total bilirubin must be less than or equal to ULN (upper limit of normal) for the lab and * alkaline phosphatase must be less than 2.5 x ULN for the lab; and * AST and ALT must be less than 2.5 x ULN for the lab. Adequate renal function within 28 days before Step 1/Study entry defined as serum creatinine less than or equal to 1.5 x ULN for the lab or measured or calculated creatinine clearance greater than or equal to 50 mL/min using the Cockroft-Gault formula for patients with creatinine levels greater than 1.5 x ULN for the lab. For Women Creatinine Clearance (mL/min) = (140 - age) x weight (kg) x 0.85 72 x serum creatinine (mg/dL) For Men Creatinine Clearance (mL/min) = (140 - age) x weight (kg) 72 x serum creatinine (mg/dL) NOTE: Adjusted body weight (AdjBW) should be used for patients that have BMI greater than or equal to 28 (less than or equal to 30% above IBW). HIV-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible for this trial. Pregnancy test (urine or serum according to institutional standard) done within 14 days before Step 1/Study entry must be negative (for women of childbearing potential only). Patients receiving a coumarin-derivative anticoagulant must agree to weekly monitoring of INR if they are randomized to Arm 1 or Arm 3 and receive capecitabine. Eligibility Criteria for Cohort A Arm-2 patients on Second Randomization Patient must have developed a ctDNA +ve assay during serial monitoring. Patient's willingness to be re-randomized affirmed. The patient must continue to have an ECOG performance status of 0 or 1. No radiographic evidence of overt metastatic disease. Pregnancy test (urine or serum according to institutional standard) done within 14 days before second randomization must be negative (for women of childbearing potential only). Adequate hematologic function within 28 days before second randomization defined as follows: * Absolute neutrophil count (ANC) must be greater than or equal to 1500/mm3; * Participants with benign ethnic neutropenia (BEN): ANC less than 1300 mm3 are eligible. * BEN (also known as constitutional neutropenia) is an inherited cause of mild or moderate neutropenia that is not associated with any increased risk for infections or other clinical manifestations. BEN is referred to as ethnic neutropenia because of its increased prevalence in people of African descent and other specific ethnic groups. * Platelet count must be greater than or equal to 100,000/mm3; and * Hemoglobin must be greater than or equal to 9 g/dL. Adequate hepatic function within 28 days before second randomization defined as follows: * total bilirubin must be less than or equal to ULN (upper limit of normal) for the lab and * alkaline phosphatase must be less than 2.5 x ULN for the lab; and * AST and ALT must be less than 2.5 x ULN for the lab. Adequate renal function within 28 days before second randomization defined as serum creatinine less than or equal to 1.5 x ULN for the lab or measured or calculated creatinine clearance greater than or equal to 50 mL/min using the Cockroft-Gault formula for patients with creatinine levels greater than 1.5 x ULN for the lab. For Women Creatinine Clearance (mL/min) = (140 - age) x weight (kg) x 0.85 72 x serum creatinine (mg/dL) For Men Creatinine Clearance (mL/min) = (140 - age) x weight (kg) 72 x serum creatinine (mg/dL)
Exclusion Criteria:
Colon cancer histology other than adenocarcinoma (i.e., neuroendocrine carcinoma, sarcoma, lymphoma, squamous cell carcinoma, etc.). Pathologic, clinical, or radiologic overt evidence of metastatic disease. This includes isolated, distant, or non-contiguous intra-abdominal metastases, even if resected. Tumor-related bowel perforation. History of prior invasive colon malignancy, regardless of disease-free interval. History of bone marrow or solid organ transplantation (regardless of current immunosuppressive therapy needs). Bone grafts, skin grafts, corneal transplants and organ/tissue donation are not exclusionary. Any prior systemic chemotherapy, targeted therapy, or immunotherapy; or radiation therapy administered as treatment for colorectal cancer (e.g., primary colon adenocarcinomas for which treatment with neoadjuvant chemotherapy and/or radiation is warranted are not permitted). EXCEPTION: one cycle of chemotherapy (regimen per treating physicians' discretion - 5-FU or capecitabine with or without oxaliplatin) is allowed but not required after consent. The optional cycle of chemotherapy should be started greater than or equal to 4 weeks from surgery and while awaiting Step 2 randomization. Other invasive malignancy within 5 years before Step 1/Study entry. Exceptions are colonic polyps, non-melanoma skin cancer or any carcinoma-in-situ. Synchronous primary rectal and/ or colon cancers. Patients with known history or current symptoms of cardiac disease, or history of treatment with cardiotoxic agents, should have a clinical risk assessment of cardiac function using the New York Heart Association Functional Classification. To be eligible for this trial, patients should be class 2B or better. Sensory or motor neuropathy greater than or equal to grade 2, according to CTCAE v5.0. Blood transfusion within two weeks before collection of blood for central ctDNA testing. Active seizure disorder uncontrolled by medication. Active or chronic infection requiring systemic therapy. Known homozygous DPD (dihydropyrimidine dehydrogenase) deficiency. Patients known to have Gilbert's Syndrome or homozygosity for UGT1A1\*28 polymorphism. Pregnancy or lactation at the time of Step 1/Study entry. Co-morbid illnesses or other concurrent disease that would make the patient inappropriate for entry into this study (i.e., unable to tolerate 6 months of combination chemotherapy or interfere significantly with the proper assessment of safety and toxicity of the prescribed regimens or prevent required follow-up). Ineligibility Criteria for Cohort A Arm-2 patients on Second Randomization Pregnancy or lactation at the time of randomization. No longer a candidate for systemic chemotherapy (FOLFOX, CAPOX, and mFOLFIRINOX) in the opinion of the treating investigator.
DEVICE: Signatera test, DRUG: mFOLFOX6 3-6 month, DRUG: CAPOX 3 month, DRUG: mFOLFIRINOX, DRUG: mFOLFOX6 6 month, DRUG: CAPOX 6 month
Stage III Colon Cancer
ctDNA positive, ctDNA negative, Adjuvant Chemotherapy, Natera, Signatera, mFOLFOX6, Stage III, CAPOX, mFOLFIRINOX, Oxaliplatin, 5-Fluorouracil (5-FU), Capecitabine, Leucovorin, Irinotecan, Stage II
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Study Locations

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AIS Cancer Center at San Joaquin Community Hospital Bakersfield, California
AMG Crystal Lake - Oncology Crystal Lake, Illinois Site Public Contact - (advocateresearch@advocate.com)
AMG Libertyville - Oncology Libertyville, Illinois Site Public Contact - (advocateresearch@advocatehealth.com)
Abbott-Northwestern Hospital Minneapolis, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Adams Cancer Center Gettysburg, Pennsylvania
Addison Gilbert Hospital Gloucester, Massachusetts
Adena Regional Medical Center Chillicothe, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Advanced Breast Care Center PLLC Warren, Michigan
AdventHealth Altamonte Altamonte Springs, Florida
AdventHealth Celebration Celebration, Florida
AdventHealth East Orlando Orlando, Florida
AdventHealth Kissimmee Kissimmee, Florida
AdventHealth Littleton Littleton, Colorado
AdventHealth Orlando Apopka, Florida Site Public Contact - (FH.Cancer.Research@flhosp.org)
AdventHealth Parker Parker, Colorado
AdventHealth Porter Denver, Colorado
AdventHealth Winter Park Winter Park, Florida
Advocate Christ Medical Center Oak Lawn, Illinois
Advocate Good Samaritan Hospital Downers Grove, Illinois Site Public Contact - (Barbara.barhamand@advocatehealth.com)
Advocate Good Shepherd Hospital Barrington, Illinois
Advocate Illinois Masonic Medical Center Chicago, Illinois
Advocate Lutheran General Hospital Park Ridge, Illinois
Advocate Outpatient Center - Aurora Aurora, Illinois Site Public Contact - (ncorp@aah.org)
Advocate Sherman Hospital Elgin, Illinois
Advocate South Suburban Hospital Hazel Crest, Illinois
Alegent Health Bergan Mercy Medical Center Omaha, Nebraska Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Alegent Health Immanuel Medical Center Omaha, Nebraska Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Alegent Health Lakeside Hospital Omaha, Nebraska Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Alegent Health Mercy Hospital Council Bluffs, Iowa
Allan Blair Cancer Centre Regina, Saskatchewan
Allegheny General Hospital Pittsburgh, Pennsylvania
Allegheny Valley Hospital Natrona Heights, Pennsylvania Site Public Contact - (Dawnmarie.DeFazio@ahn.org)
Alta Bates Summit Medical Center-Herrick Campus Berkeley, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Altru Cancer Center Grand Forks, North Dakota
American Fork Hospital / Huntsman Intermountain Cancer Center American Fork, Utah Site Public Contact - (officeofresearch@imail.org)
Armes Family Cancer Center Findlay, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Arnold Palmer Cancer Center Medical Oncology Norwin N. Huntingdon, Pennsylvania Site Public Contact - (ClinicalResearchServices@upmc.edu)
Arthur J E Child Comprehensive Cancer Centre Calgary, Alberta Site Public Contact - (Roster@nrgoncology.org)
Ascension All Saints Hospital Racine, Wisconsin Site Public Contact - (AWRI.Inquiry@Ascension.org)
Ascension Calumet Hospital Chilton, Wisconsin Site Public Contact - (AWRI.inquiry@ascension.org)
Ascension Columbia Saint Mary's Hospital - Milwaukee Milwaukee, Wisconsin Site Public Contact - (AWRI.Inquiry@Ascension.org)
Ascension Columbia Saint Mary's Hospital Ozaukee Mequon, Wisconsin Site Public Contact - (AWRI.Inquiry@Ascension.org)
Ascension Medical Group Southeast Wisconsin - Mayfair Road Wauwatosa, Wisconsin Site Public Contact - (AWRI.Inquiry@Ascension.org)
Ascension Mercy Hospital Oshkosh, Wisconsin Site Public Contact - (AWRI.inquiry@ascension.org)
Ascension Saint Elizabeth Hospital Appleton, Wisconsin Site Public Contact - (AWRI.inquiry@ascension.org)
Ascension Saint Francis - Reiman Cancer Center Franklin, Wisconsin Site Public Contact - (AWRI.Inquiry@Ascension.org)
Ascension Southeast Wisconsin Hospital - Elmbrook Campus Brookfield, Wisconsin Site Public Contact - (AWRI.Inquiry@Ascension.org)
Ascension Via Christi Hospitals Wichita Wichita, Kansas Site Public Contact - (research@viachristi.org)
Aspirus Cancer Care - James Beck Cancer Center Rhinelander, Wisconsin Site Public Contact - (Beth.Knetter@aspirus.org)
Aspirus Cancer Care - Stevens Point Stevens Point, Wisconsin Site Public Contact - (Beth.Knetter@aspirus.org)
Aspirus Cancer Care - Wisconsin Rapids Wisconsin Rapids, Wisconsin
Aspirus Medford Hospital Medford, Wisconsin Site Public Contact - (Beth.Knetter@aspirus.org)
Aspirus Regional Cancer Center Wausau, Wisconsin
Asplundh Cancer Pavilion Willow Grove, Pennsylvania Site Public Contact - (ONCTrialNow@jefferson.edu)
AtlantiCare Health Park-Cape May Court House Cape May Court House, New Jersey
AtlantiCare Surgery Center Egg Harbor, New Jersey
Atlantic Health Sciences Corporation-Saint John Regional Hospital Saint John, New Brunswick
Atrium Health Cabarrus/LCI-Concord Concord, North Carolina
Atrium Health Pineville/LCI-Pineville Charlotte, North Carolina
Atrium Health Union/LCI-Union Monroe, North Carolina
Atrium Health University City/LCI-University Charlotte, North Carolina
Atrium Medical Center-Middletown Regional Hospital Franklin, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Aultman Alliance Community Hospital Alliance, Ohio
Aultman Health Foundation Canton, Ohio Site Public Contact - (ClinicalReserachDept@aultman.com)
Aurora Bay Area Medical Group-Marinette Marinette, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora BayCare Medical Center Green Bay, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Cancer Care-Grafton Grafton, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Cancer Care-Kenosha South Kenosha, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Cancer Care-Milwaukee Milwaukee, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Cancer Care-Milwaukee West Wauwatosa, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Cancer Care-Racine Racine, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Cancer Care-Southern Lakes VLCC Burlington, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Health Care Germantown Health Center Germantown, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Medical Center in Summit Summit, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Saint Luke's Medical Center Milwaukee, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Saint Luke's South Shore Cudahy, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora Sinai Medical Center Milwaukee, Wisconsin Site Public Contact - (ncorp@aurora.org)
Aurora West Allis Medical Center West Allis, Wisconsin Site Public Contact - (ncorp@aurora.org)
Avera Cancer Institute Sioux Falls, South Dakota Site Public Contact - (OncRegulatory@avera.org)
Avera Cancer Institute - Mitchell Mitchell, South Dakota Site Public Contact - (OncRegulatory@avera.org)
Avera Cancer Institute at Pierre Pierre, South Dakota Site Public Contact - (OncRegulatory@avera.org)
Avera Cancer Institute at Yankton Yankton, South Dakota Site Public Contact - (OncRegulatory@avera.org)
Avera Cancer Institute-Aberdeen Aberdeen, South Dakota Site Public Contact - (oncregulatory@avera.org)
BASS Medical Group - Lennon Walnut Creek, California Site Public Contact - (brenna.lindsey@bassmedicalgroup.com)
BCCA-Cancer Centre for the North Prince George, British Columbia
BCCA-Vancouver Cancer Centre Vancouver, British Columbia
BCCA-Vancouver Island Cancer Centre Victoria, British Columbia
BJC Outpatient Center at Sunset Hills Sunset Hills, Missouri
Banner University Medical Center - Tucson Tucson, Arizona Site Public Contact - (UACC-IIT@uacc.arizona.edu)
Baptist Cancer Center-Grenada Grenada, Mississippi Site Public Contact - (BCCclintrials@bmhcc.org)
Baptist Health Hamburg Lexington, Kentucky
Baptist Health Lexington Lexington, Kentucky
Baptist Memorial Hospital and Cancer Center-Collierville Collierville, Tennessee Site Public Contact - (BCCclintrials@bmhcc.org)
Baptist Memorial Hospital and Cancer Center-Desoto Southhaven, Mississippi Site Public Contact - (BCCclintrials@bmhcc.org)
Baptist Memorial Hospital and Cancer Center-Golden Triangle Columbus, Mississippi Site Public Contact - (BCCclintrials@bmhcc.org)
Baptist Memorial Hospital and Cancer Center-Memphis Memphis, Tennessee Site Public Contact - (BCCclintrials@bmhcc.org)
Baptist Memorial Hospital and Cancer Center-Oxford Oxford, Mississippi Site Public Contact - (BCCclintrials@bmhcc.org)
Baptist Memorial Hospital and Cancer Center-Union County New Albany, Mississippi Site Public Contact - (BCCclintrials@bmhcc.org)
Bay Area Tumor Institute Oakland, California
Bayhealth Hospital Kent Campus Dover, Delaware
Bayhealth Hospital Sussex Campus Milford, Delaware
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center Houston, Texas Site Public Contact - (burton@bcm.edu)
Beacon Kalamazoo Cancer Center Kalamazoo, Michigan
Ben Taub General Hospital Houston, Texas
Benefis Sletten Cancer Institute Great Falls, Montana Site Public Contact - (mccinfo@mtcancer.org)
Beth Israel Deaconess Medical Center/Winchester Center for Cancer Care Winchester, Massachusetts
Bethesda North Hospital Cincinnati, Ohio Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Beverly Hospital Beverly, Massachusetts
Bhadresh Nayak MD PC-Sterling Heights Sterling Heights, Michigan
Billings Clinic Cancer Center Billings, Montana Site Public Contact - (research@billingsclinic.org)
Blanchard Valley Hospital Findlay, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Bon Secours Memorial Regional Medical Center Mechanicsville, Virginia Site Public Contact - (anne_carmellat@bshsi.org)
Bon Secours Richmond Community Hospital Richmond, Virginia Site Public Contact - (anne_carmellat@bshsi.org)
Bon Secours Saint Francis Hospital Charleston, South Carolina Site Public Contact - (Julia.Johnson@rsfh.com)
Bon Secours Saint Francis Medical Center Midlothian, Virginia Site Public Contact - (anne_carmellat@bshsi.org)
Bon Secours Saint Mary's Hospital Richmond, Virginia Site Public Contact - (anne_carmellat@bshsi.org)
Boston Medical Center Boston, Massachusetts
Bozeman Health Deaconess Hospital Bozeman, Montana Site Public Contact - (mccinfo@mtcancer.org)
Bronson Battle Creek Battle Creek, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Bronson Methodist Hospital Kalamazoo, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
CHI Health Good Samaritan Kearney, Nebraska Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
CHI Saint Vincent Cancer Center Hot Springs Hot Springs, Arkansas
CHU de Quebec-L'Hotel-Dieu de Quebec (HDQ) Québec, Quebec Site Public Contact - (rechclinique@crchuq.ulaval.ca)
CIUSSSEMTL-Hopital Maisonneuve-Rosemont Montreal, Quebec
CSSS Champlain-Charles Le Moyne Greenfield Park, Quebec
CTCA at Southeastern Regional Medical Center Newnan, Georgia
California Pacific Medical Center-Pacific Campus San Francisco, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Cambridge Medical Center Cambridge, Minnesota
Cambridge Memorial Hospital Cambridge, Ontario
Camden Clark Medical Center Parkersburg, West Virginia Site Public Contact - (cancertrialsinfo@hsc.wvu.edu)
Cancer Care Associates of York York, Pennsylvania
Cancer Care Center of O'Fallon O'Fallon, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Care Specialists of Illinois - Decatur Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Care and Hematology-Fort Collins Fort Collins, Colorado Site Public Contact - (Roster@nrgoncology.org)
Cancer Center at Saint Joseph's Phoenix, Arizona Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Cancer Center of Kansas-Wichita Medical Arts Tower Wichita, Kansas Site Public Contact - (research@viachristi.org)
Cancer Center of Western Wisconsin New Richmond, Wisconsin Site Public Contact - (mmcorc@healthpartners.com)
Cancer Centers of Southwest Oklahoma Research Lawton, Oklahoma
Cancer Hematology Centers - Flint Flint, Michigan Site Public Contact - (wstrong@ghci.org)
Cancer Partners of Nebraska Lincoln, Nebraska Site Public Contact - (research@cancerpartners.com)
Cancer Specialists of Tidewater Limited Chesapeake, Virginia Site Public Contact - (casey.morris@rivhs.com)
Cancer Specialists of Tidewater-Suffolk Suffolk, Virginia Site Public Contact - (casey.morris@rivhs.com)
Cancer and Hematology Centers of Western Michigan - Norton Shores Norton Shores, Michigan Site Public Contact - (connie.szczepanek@crcwm.org)
Carle Cancer Center Urbana, Illinois Site Public Contact - (Research@carle.com)
Carle Physician Group-Effingham Effingham, Illinois Site Public Contact - (Research@carle.com)
Carle Physician Group-Mattoon/Charleston Mattoon, Illinois Site Public Contact - (Research@carle.com)
Carle at The Riverfront Danville, Illinois Site Public Contact - (Research@Carle.com)
Carlisle Regional Cancer Center Carlisle, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
Caro Cancer Center Caro, Michigan
CaroMont Regional Medical Center Gastonia, North Carolina Site Public Contact - (tammy.cozad@caromonthealth.org)
Carolinas Medical Center/Levine Cancer Institute Charlotte, North Carolina
Carson Tahoe Regional Medical Center Carson City, Nevada Site Public Contact - (research@sncrf.org)
Case Western Reserve University Cleveland, Ohio
Cedars Sinai Medical Center Los Angeles, California
Centra Alan B Pearson Regional Cancer Center Lynchburg, Virginia Site Public Contact - (Kevin.Patel@centrahealth.com)
Central Care Cancer Center - Bolivar Bolivar, Missouri Site Public Contact - (aroland@kccop.org)
Central Care Cancer Center - Garden City Garden City, Kansas Site Public Contact - (aroland@kccop.org)
Central Care Cancer Center - Great Bend Great Bend, Kansas Site Public Contact - (aroland@kccop.org)
Central Ohio Breast and Endocrine Surgery Gahanna, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Central Vermont Medical Center/National Life Cancer Treatment Berlin Corners, Vermont
Centralia Oncology Clinic Centralia, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Centre Hospitalier Universitaire de Sherbrooke-Fleurimont Sherbrooke, Quebec Site Public Contact - (crcinformation.chus@ssss.gouv.qc.ca)
Centro Comprensivo de Cancer de UPR San Juan, Site Public Contact - (Roster@nrgoncology.org)
Charleston Oncology - Roper Charleston, South Carolina Site Public Contact - (Julia.Johnson@rsfh.com)
Charleston Oncology - Saint Francis Charleston, South Carolina Site Public Contact - (Julia.Johnson@rsfh.com)
Chelsea Hospital Chelsea, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Chester County Hospital West Chester, Pennsylvania
City of Hope Antelope Valley Lancaster, California
City of Hope Comprehensive Cancer Center Duarte, California Site Public Contact - (becomingapatient@coh.org)
City of Hope South Bay Torrance, California
City of Hope South Pasadena South Pasadena, California Site Public Contact - (becomingapatient@coh.org)
City of Hope Upland Upland, California Site Public Contact - (becomingapatient@coh.org)
City of Hope at Irvine Lennar Irvine, California
Clackamas Radiation Oncology Center Clackamas, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Cleveland Clinic Akron General Akron, Ohio Site Public Contact - (CancerAnswer@ccf.org)
Cleveland Clinic Cancer Center Independence Independence, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Cleveland Clinic Cancer Center Mansfield Mansfield, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Cleveland Clinic Cancer Center Strongsville Strongsville, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Cleveland Clinic Cancer Center/Fairview Hospital Cleveland, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Cleveland Clinic Foundation Cleveland, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Cleveland Clinic Mercy Hospital Canton, Ohio
Cleveland Clinic Wooster Family Health and Surgery Center Wooster, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Cleveland Clinic-Weston Weston, Florida
Coborn Cancer Center at Saint Cloud Hospital Saint Cloud, Minnesota Site Public Contact - (coborncancercenter@centracare.com)
Columbus Oncology and Hematology Associates Dublin, Ohio
Columbus Oncology and Hematology Associates Inc Columbus, Ohio
CommonSpirit Cancer Center Mercy Durango, Colorado Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Commonwealth Cancer Center-Corbin Corbin, Kentucky Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Community Hospital of Anaconda Anaconda, Montana Site Public Contact - (mccinfo@mtcancer.org)
Community Medical Center Missoula, Montana Site Public Contact - (mccinfo@mtcancer.org)
Community Medical Center Missoula, Montana Site Public Contact - (Lennette.Gonzales@rwjbh.org)
Community Medical Center Missoula, Montana Site Public Contact - (HemonCCTrials@geisinger.edu)
Comprehensive Cancer Centers of Nevada Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
Comprehensive Cancer Centers of Nevada - Central Valley Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
Comprehensive Cancer Centers of Nevada - Henderson Henderson, Nevada Site Public Contact - (research@sncrf.org)
Condell Memorial Hospital Libertyville, Illinois Site Public Contact - (advocateresearch@advocatehealth.com)
Cone Health Cancer Center Greensboro, North Carolina Site Public Contact - (stacey.phelps@conehealth.com)
Contra Costa Regional Medical Center Martinez, California
Corewell Health Beaumont Troy Hospital Troy, Michigan
Corewell Health Dearborn Hospital Dearborn, Michigan
Corewell Health Grand Rapids Hospitals - Butterworth Hospital Grand Rapids, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center Saint Joseph, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health Reed City Hospital Reed City, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health William Beaumont University Hospital Royal Oak, Michigan
Covenant Health Cancer Centers Knoxville, Tennessee
Covenant Health Cancer Centers - West Knoxville, Tennessee
Covenant Health Oncology Group - Oak Ridge Oak Ridge, Tennessee
Cox Cancer Center Branson Branson, Missouri
CoxHealth South Hospital Springfield, Missouri
Creighton University Medical Center Omaha, Nebraska Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Crossroads Cancer Center Effingham, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Dana Farber-Merrimack Valley Methuen, Massachusetts
Dana-Farber Cancer Institute at Boston Medical Center - Brighton Brighton, Massachusetts
Dana-Farber Cancer Institute at Foxborough Foxborough, Massachusetts
Dana-Farber/Brigham and Women's Cancer Center at Milford Regional Milford, Massachusetts
Dana-Farber/Brigham and Women's Cancer Center at South Shore South Weymouth, Massachusetts
Dartmouth Cancer Center - North Saint Johnsbury, Vermont Site Public Contact - (cancer.research.nurse@hitchcock.org)
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center Lebanon, New Hampshire Site Public Contact - (cancer.research.nurse@dartmouth.edu)
Dayton Physician LLC - Englewood Dayton, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Dayton Physicians LLC - Troy Troy, Ohio
Dayton Physicians LLC-Atrium Franklin, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Dayton Physicians LLC-Miami Valley South Centerville, Ohio
Dayton Physicians LLC-Wayne Greenville, Ohio
Decatur Memorial Hospital Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Delaware Health Center-Grady Cancer Center Delaware, Ohio
Dell Seton Medical Center at The University of Texas Austin, Texas
Denver Health Medical Center Denver, Colorado Site Public Contact - (ccrp@co-cancerresearch.org)
Dillon Health Center/Shaw Cancer Center Dillon, Colorado
Divine Providence Hospital Williamsport, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
Doctors Cancer Center Manati,
Doctors Hospital Columbus, Ohio
Drexel Town Square Health Center Oak Creek, Wisconsin
Dublin Methodist Hospital Dublin, Ohio
Duke Cancer Center Cary Cary, North Carolina Site Public Contact - (NCTNStudyTeam@dm.duke.edu)
Duke Cancer Center Raleigh Raleigh, North Carolina Site Public Contact - (NCTNStudyTeam@dm.duke.edu)
Duke University Medical Center Durham, North Carolina
Duluth Clinic Ashland Ashland, Wisconsin Site Public Contact - (CancerTrials@EssentiaHealth.org)
East Carolina University Greenville, North Carolina Site Public Contact - (eubankss@ecu.edu)
Eden Hospital Medical Center Castro Valley, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Edward Hines Jr VA Hospital Hines, Illinois
Edward Hospital/Cancer Center Naperville, Illinois
Edward Hospital/Cancer Center?Plainfield Plainfield, Illinois Site Public Contact - (Cancerresearch@edward.org)
Eisenhower Army Medical Center Fort Gordon, Georgia
Eisenhower Medical Center Rancho Mirage, California
Elmhurst Memorial Hospital Elmhurst, Illinois Site Public Contact - (Jrohde@emhc.org)
Enloe Medical Center Chico, California
Ephrata Cancer Center Ephrata, Pennsylvania
Epic Care Cyberknife Center Walnut Creek, California
Epic Care Partners in Cancer Care Emeryville, California
Epic Care-Dublin Dublin, California
Essentia Health - Deer River Clinic Deer River, Minnesota Site Public Contact - (CancerTrials@EssentiaHealth.org)
Essentia Health - Moose Lake Clinic Moose Lake, Minnesota
Essentia Health Cancer Center Duluth, Minnesota Site Public Contact - (CancerTrials@EssentiaHealth.org)
Essentia Health Cancer Center-South University Clinic Fargo, North Dakota Site Public Contact - (CancerTrials@EssentiaHealth.org)
Essentia Health Hibbing Clinic Hibbing, Minnesota
Essentia Health Saint Joseph's Medical Center Brainerd, Minnesota Site Public Contact - (CancerTrials@EssentiaHealth.org)
Essentia Health Saint Mary's - Detroit Lakes Clinic Detroit Lakes, Minnesota Site Public Contact - (CancerTrials@EssentiaHealth.org)
Essentia Health Sandstone Sandstone, Minnesota Site Public Contact - (CancerTrials@EssentiaHealth.org)
Essentia Health Virginia Clinic Virginia, Minnesota Site Public Contact - (CancerTrials@EssentiaHealth.org)
Exeter Hospital Exeter, New Hampshire
FHCC Overlake Bellevue, Washington
FHCC at EvergreenHealth Kirkland, Washington
FHCC at Northwest Hospital Seattle, Washington
FMH James M Stockman Cancer Institute Frederick, Maryland
Fairfield Medical Center Lancaster, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Fairview Clinics and Surgery Center Maple Grove Maple Grove, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Fairview Lakes Medical Center Wyoming, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Fairview Northland Medical Center Princeton, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Fairview Ridges Hospital Burnsville, Minnesota
Fairview Southdale Hospital Edina, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Farmington Health Center Farmington, Utah Site Public Contact - (cancerinfo@hci.utah.edu)
FirstHealth of the Carolinas-Moore Regional Hospital Pinehurst, North Carolina Site Public Contact - (jcwilliams@firsthealth.org)
Flaget Memorial Hospital Bardstown, Kentucky Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Forbes Hospital Monroeville, Pennsylvania
Fox Chase Cancer Center Philadelphia, Pennsylvania
Franciscan Research Center-Northwest Medical Plaza Tacoma, Washington
Fred Hutchinson Cancer Center Seattle, Washington
Frederick Memorial Hospital Frederick, Maryland
Freeman Health System Joplin, Montana Site Public Contact - (LJCrockett@freemanhealth.com)
Fremont - Rideout Cancer Center Marysville, California
Froedtert Menomonee Falls Hospital Menomonee Falls, Wisconsin
Froedtert West Bend Hospital/Kraemer Cancer Center West Bend, Wisconsin
Garnet Health Medical Center Middletown, New York Site Public Contact - (jgerlach@garnethealth.org)
Geauga Hospital Chardon, Ohio
Geisinger Medical Center Danville, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Geisinger Medical Center-Cancer Center Hazleton Hazleton, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Geisinger Medical Oncology-Lewisburg Lewisburg, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Geisinger Wyoming Valley/Henry Cancer Center Wilkes-Barre, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Gene Upshaw Memorial Tahoe Forest Cancer Center Truckee, California
Genesee Hematology Oncology PC Flint, Michigan Site Public Contact - (wstrong@ghci.org)
Genesis Healthcare System Cancer Care Center Zanesville, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Genesys Hurley Cancer Institute Flint, Michigan Site Public Contact - (wstrong@ghci.org)
George Washington University Medical Center Washington D.C., District of Columbia
Gibbs Cancer Center-Gaffney Gaffney, South Carolina Site Public Contact - (kmertz-rivera@gibbscc.org)
Gibbs Cancer Center-Pelham Greer, South Carolina Site Public Contact - (kmertz-rivera@gibbscc.org)
Glens Falls Hospital Glens Falls, New York
Good Samaritan Hospital - Cincinnati Cincinnati, Ohio Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Grady Memorial Hospital Delaware, Ohio
Grand Valley Oncology Grand Junction, Colorado Site Public Contact - (gvoclinicaltrials@gjhosp.org)
Grand View Hospital Sellersville, Pennsylvania
Grant Medical Center Columbus, Ohio
Great Falls Clinic Great Falls, Montana Site Public Contact - (mccinfo@mtcancer.org)
Greater Baltimore Medical Center Baltimore, Maryland
Greater Dayton Cancer Center Kettering, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Greater Regional Medical Center Creston, Iowa
Gundersen Lutheran Medical Center La Crosse, Wisconsin Site Public Contact - (cancerctr@gundersenhealth.org)
HSHS Sacred Heart Hospital Eau Claire, Wisconsin
Harold Alfond Center for Cancer Care Augusta, Maine
Hawaii Cancer Care - Westridge ‘Aiea, Hawaii Site Public Contact - (info@hawaiicancercare.com)
Hawaii Cancer Care Inc - Waterfront Plaza Honolulu, Hawaii Site Public Contact - (i.webster@hawaiicancercare.com)
Health Partners Inc Minneapolis, Minnesota
Heartland Regional Medical Center Saint Joseph, Missouri Site Public Contact - (Trisha.England2@mymlc.com)
Helen F Graham Cancer Center Newark, Delaware Site Public Contact - (lbarone@christianacare.org)
Hematology Oncology Consultants-Clarkston Clarkston, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Hennepin County Medical Center Minneapolis, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Henry Ford Health Providence Novi Hospital Novi, Michigan Site Public Contact - (kfife3@hfhs.org)
Henry Ford Health Providence Southfield Hospital Southfield, Michigan Site Public Contact - (kfife3@hfhs.org)
Henry Ford Health Saint John Hospital Detroit, Michigan Site Public Contact - (Kkeenan1@hfhs.org)
Henry Ford Health Warren Hospital Warren, Michigan Site Public Contact - (kforman1@hfhs.org)
Henry Ford Madison Heights Hospital - Breast Warren, Michigan Site Public Contact - (kforman1@hfhs.org)
Henry Ford River District Hospital East China Township, Michigan Site Public Contact - (kforman1@hfhs.org)
Henry Ford Saint John Hospital - Academic Grosse Pointe Woods, Michigan Site Public Contact - (kforman1@hfhs.org)
Henry Ford Saint John Hospital - Breast Grosse Pointe Woods, Michigan Site Public Contact - (karen.forman@ascension.org)
Henry Ford Saint John Hospital - Macomb Medical Macomb, Michigan Site Public Contact - (kforman1@hfhs.org)
Henry Ford Saint John Hospital - Van Elslander Grosse Pointe Woods, Michigan Site Public Contact - (kforman1@hfhs.org)
Henry Ford Warren Hospital - Breast Macomb Macomb, Michigan Site Public Contact - (kforman1@hfhs.org)
Henry Ford Warren Hospital - GLCMS Warren, Michigan Site Public Contact - (kforman1@hfhs.org)
Highline Medical Center-Main Campus Burien, Washington
Hillcrest Hospital Cancer Center Mayfield Heights, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Holy Cross Hospital Silver Spring, Maryland Site Public Contact - (eileen.georgi@holy-cross.com)
Hope Cancer Center Pontiac, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Hopital du Sacre-Coeur de Montreal Montreal, Quebec
Hotel-Dieu de Levis Lévis, Quebec Site Public Contact - (ctsucontact@westat.com)
Humber River Hospital Toronto, Ontario Site Public Contact - (research@hrh.ca)
Huntsman Cancer Institute/University of Utah Salt Lake City, Utah Site Public Contact - (cancerinfo@hci.utah.edu)
Hurley Medical Center Flint, Michigan Site Public Contact - (wstrong@ghci.org)
Huron Gastroenterology PC Ypsilanti, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
IRMC Cancer Center Indiana, Pennsylvania Site Public Contact - (haneydl@upmc.edu)
Illinois CancerCare - Washington Washington, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Bloomington Bloomington, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Canton Canton, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Carthage Carthage, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Dixon Dixon, Illinois
Illinois CancerCare-Eureka Eureka, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Galesburg Galesburg, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Kewanee Clinic Kewanee, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Macomb Macomb, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Ottawa Clinic Ottawa, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Pekin Pekin, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Peoria Peoria, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Peru Peru, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Illinois CancerCare-Princeton Princeton, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Indu and Raj Soin Medical Center Beavercreek, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Ingalls Memorial Hospital Harvey, Illinois Site Public Contact - (clinicaltrials@ingalls.org)
Integris Cancer Institute of Oklahoma Oklahoma City, Oklahoma
Integris Southwest Medical Center Oklahoma City, Oklahoma Site Public Contact - (Roster@nrgoncology.org)
Intermountain Health Platte Valley Hospital Brighton, Colorado Site Public Contact - (peaksresearch@imail.org)
Intermountain Medical Center Murray, Utah Site Public Contact - (officeofresearch@imail.org)
Iowa Methodist Medical Center Des Moines, Iowa
Jefferson Cherry Hill Hospital Cherry Hill, New Jersey Site Public Contact - (ONCTrialNow@jefferson.edu)
Jefferson Hospital Jefferson Hills, Pennsylvania Site Public Contact - (ddefazio@wpahs.org)
Jefferson Methodist Hospital Philadelphia, Pennsylvania Site Public Contact - (ONCTrialNow@jefferson.edu)
Jefferson Torresdale Hospital Philadelphia, Pennsylvania Site Public Contact - (ONCTrialNow@jefferson.edu)
Jersey City Medical Center Jersey City, New Jersey Site Public Contact - (Roster@nrgoncology.org)
Jewish General Hospital Montreal, Quebec
Jewish Hospital Louisville, Kentucky
Jewish Hospital Medical Center South Shepherdsville, Kentucky
John H Stroger Jr Hospital of Cook County Chicago, Illinois
John Muir Medical Center-Walnut Creek Walnut Creek, California Site Public Contact - (clinicalresearch@johnmuirhealth.com)
Jupiter Medical Center Jupiter, Florida
Juravinski Cancer Centre at Hamilton Health Sciences Hamilton, Ontario
Kadlec Clinic Hematology and Oncology Kennewick, Washington Site Public Contact - (research@kadlecmed.org)
Kaiser Permanente - Largo Medical Center Largo, Maryland Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser Permanente - Panorama City Panorama City, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente Downtown Commons Sacramento, California Site Public Contact - (kpoct@kp.org)
Kaiser Permanente Dublin Dublin, California
Kaiser Permanente Fresno Orchard Plaza Fresno, California
Kaiser Permanente Los Angeles Medical Center Los Angeles, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente Lutherville - Timonium Medical Center Lutherville, Maryland Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser Permanente Medical Center - Santa Clara Santa Clara, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente Medical Center-Vacaville Vacaville, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente Moanalua Medical Center Honolulu, Hawaii Site Public Contact - (shelley.a.clark@kp.org)
Kaiser Permanente Northwest Portland, Oregon Site Public Contact - (information@kpchr.org)
Kaiser Permanente San Leandro San Leandro, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente South Bay Harbor City, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente Tysons Corner Medical Center McLean, Virginia Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser Permanente West Los Angeles Los Angeles, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente- Marshall Medical Offices Redwood City, California
Kaiser Permanente- Modesto MOB II Modesto, California
Kaiser Permanente-Anaheim Anaheim, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Baldwin Park Baldwin Park, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Bellflower Bellflower, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Burke Medical Center Burke, Virginia Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser Permanente-Capitol Hill Medical Center Washington D.C., District of Columbia Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser Permanente-Caton Hill Medical Center Woodbridge, Virginia Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser Permanente-Deer Valley Medical Center Antioch, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Fontana Fontana, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Franklin Denver, Colorado Site Public Contact - (KPCOIHRClinicalResearch@kp.org)
Kaiser Permanente-Fremont Fremont, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Fresno Fresno, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Gaithersburg Medical Center Gaithersburg, Maryland Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser Permanente-Irvine Irvine, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Lone Tree Lone Tree, Colorado Site Public Contact - (KPCOIHRClinicalResearch@kp.org)
Kaiser Permanente-Modesto Modesto, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Oakland Oakland, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Ontario Ontario, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Richmond Richmond, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Riverside Riverside, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Rock Creek Lafayette, Colorado Site Public Contact - (KPCOIHRClinicalResearch@kp.org)
Kaiser Permanente-Roseville Roseville, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-San Diego Zion San Diego, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-San Francisco San Francisco, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-San Marcos San Marcos, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Santa Rosa Santa Rosa, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Santa Teresa-San Jose San Jose, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-South Sacramento Sacramento, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-South San Francisco South San Francisco, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Stockton Stockton, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Vallejo Vallejo, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Walnut Creek Walnut Creek, California Site Public Contact - (Kpoct@kp.org)
Kaiser Permanente-Woodland Hills Woodland Hills, California Site Public Contact - (clinical.trials@kp.org)
Kaiser Permanente-Woodlawn Medical Center Baltimore, Maryland Site Public Contact - (Charmaine.A.Mckie@kp.org)
Kaiser San Rafael-Gallinas San Rafael, California Site Public Contact - (Kpoct@kp.org)
Keck Medicine of USC Koreatown Los Angeles, California
Kettering Medical Center Kettering, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Kingman Regional Medical Center Kingman, Arizona Site Public Contact - (research@sncrf.org)
Kingston Health Sciences Centre Kingston, Ontario Site Public Contact - (cc-clinicaltrials@kgh.kari.net)
Knox Community Hospital Mount Vernon, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Kootenai Clinic Cancer Services - Post Falls Post Falls, Idaho Site Public Contact - (mccinfo@mtcancer.org)
Kootenai Clinic Cancer Services - Sandpoint Sandpoint, Idaho Site Public Contact - (mccinfo@mtcancer.org)
Kootenai Health - Coeur d'Alene Coeur d'Alene, Idaho Site Public Contact - (mccinfo@mtcancer.org)
LDS Hospital Salt Lake City, Utah Site Public Contact - (officeofresearch@imail.org)
LSU Health Baton Rouge-North Clinic Baton Rouge, Louisiana Site Public Contact - (research@ololrmc.com)
Lahey Hospital and Medical Center Burlington, Massachusetts Site Public Contact - (lhmc-cancer-clinical-trials@lahey.org)
Lahey Medical Center-Peabody Peabody, Massachusetts Site Public Contact - (lhmc-cancer-clinical-trials@lahey.org)
Lakeridge Health Oshawa Oshawa, Ontario
Lakeview Hospital Stillwater, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Lancaster General Ann B Barshinger Cancer Institute Lancaster, Pennsylvania
Lancaster General Hospital Lancaster, Pennsylvania
Langlade Hospital and Cancer Center Antigo, Wisconsin Site Public Contact - (Juli.Alford@aspirus.org)
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York, New York
Legacy Cancer Institute Medical Oncology and Day Treatment Vancouver, Washington Site Public Contact - (oncologyresearch@lhs.org)
Legacy Good Samaritan Hospital and Medical Center Portland, Oregon Site Public Contact - (cancer@lhs.org)
Legacy Meridian Park Hospital Tualatin, Oregon
Legacy Mount Hood Medical Center Gresham, Oregon
Legacy Salmon Creek Hospital Vancouver, Washington
Lehigh Valley Hospital - Muhlenberg Bethlehem, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Lehigh Valley Hospital-Cedar Crest Allentown, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Lehigh Valley Hospital-Hazleton Hazleton, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Lenox Hill Hospital New York, New York
Levine Cancer Institute-Ballantyne Charlotte, North Carolina
Levine Cancer Institute-SouthPark Charlotte, North Carolina
Licking Memorial Hospital Newark, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Logan Health Medical Center Kalispell, Montana Site Public Contact - (mccinfo@mtcancer.org)
Logan Regional Hospital Logan, Utah Site Public Contact - (officeofresearch@imail.org)
Loma Linda University Medical Center Murrieta, California
London Regional Cancer Program London, Ontario
Long Beach Memorial Medical Center-Todd Cancer Institute Long Beach, California
Longmont United Hospital Longmont, Colorado Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Los Angeles General Medical Center Los Angeles, California Site Public Contact - (uscnorrisinfo@med.usc.edu)
Louisiana State University Health Science Center New Orleans, Louisiana Site Public Contact - (emede1@lsuhsc.edu)
Loyola University Medical Center Maywood, Illinois
Lutheran Hospital - Cancer Centers of Colorado Golden, Colorado Site Public Contact - (peaksresearch@imail.org)
Lyndon Baines Johnson General Hospital Houston, Texas
M D Anderson Cancer Center Houston, Texas Site Public Contact - (askmdanderson@mdanderson.org)
MD Anderson League City League City, Texas Site Public Contact - (askmdanderson@mdanderson.org)
MD Anderson West Houston Houston, Texas Site Public Contact - (askmdanderson@mdanderson.org)
MD Anderson in Sugar Land Sugar Land, Texas Site Public Contact - (askmdanderson@mdanderson.org)
MD Anderson in The Woodlands Conroe, Texas Site Public Contact - (askmdanderson@mdanderson.org)
MU Health - University Hospital/Ellis Fischel Cancer Center Columbia, Missouri
MU Health Care Goldschmidt Cancer Center Jefferson City, Missouri
Macomb Hematology Oncology PC Warren, Michigan
MaineHealth Cancer Care Center of York County Sanford, Maine
MaineHealth Cancer Care and IV Therapy - Sanford Sanford, Maine Site Public Contact - (clinicalresearch@mainehealth.org)
MaineHealth Cancer Care and IV Therapy - South Portland South Portland, Maine Site Public Contact - (clinicalresearch@mainehealth.org)
MaineHealth Maine Medical Center - Biddeford Biddeford, Maine
Manhattan Eye Ear and Throat Hospital New York, New York
Margaret R Pardee Memorial Hospital Hendersonville, North Carolina Site Public Contact - (pardeecancerresearch@unchealth.unc.edu)
Marietta Memorial Hospital Marietta, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Markham Stouffville Hospital Markham, Ontario Site Public Contact - (ctsucontact@westat.com)
Marshall Cancer Center Cameron Park, California Site Public Contact - (cancerservices@marshallmedical.org)
Marshfield Clinic - Wisconsin Rapids Center Wisconsin Rapids, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Clinic-Chippewa Center Chippewa Falls, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Clinic-Wausau Center Wausau, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center - Ladysmith Ladysmith, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center - Minocqua Minocqua, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center - Neillsville Neillsville, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center - Weston Weston, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-EC Cancer Center Eau Claire, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-Marshfield Marshfield, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-Rice Lake Rice Lake, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Marshfield Medical Center-River Region at Stevens Point Stevens Point, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Mary Greeley Medical Center Ames, Iowa
Mayo Clinic Health System-Eau Claire Clinic Eau Claire, Wisconsin
Mayo Clinic Health System-Franciscan Healthcare La Crosse, Wisconsin
Mayo Clinic Hospital in Arizona Phoenix, Arizona
Mayo Clinic in Rochester Rochester, Minnesota
McFarland Clinic - Ames Ames, Iowa Site Public Contact - (ksoder@mcfarlandclinic.com)
McFarland Clinic - Boone Boone, Iowa
McFarland Clinic - Jefferson Jefferson, Iowa
McFarland Clinic - Marshalltown Marshalltown, Iowa
McFarland Clinic - Trinity Cancer Center Fort Dodge, Iowa
McKay-Dee Hospital Center Ogden, Utah Site Public Contact - (officeofresearch@imail.org)
MedStar Franklin Square Medical Center/Weinberg Cancer Institute Baltimore, Maryland
MedStar Georgetown University Hospital Washington D.C., District of Columbia
MedStar Good Samaritan Hospital Baltimore, Maryland Site Public Contact - (Barbara.rector@medstar.net)
Medical Center of Baton Rouge Baton Rouge, Louisiana Site Public Contact - (Camille.Beck@Ochsner.org)
Medical Center of the Rockies Loveland, Colorado
Medical College of Wisconsin Milwaukee, Wisconsin
Medical Oncology Hematology Consultants PA Newark, Delaware Site Public Contact - (lbarone@christianacare.org)
Medical University of South Carolina Charleston, South Carolina Site Public Contact - (hcc-clinical-trials@musc.edu)
Medstar Washington Hospital Center Washington D.C., District of Columbia
Memorial Health University Medical Center Savannah, Georgia Site Public Contact - (Lorraine.OHara@hcahealthcare.com)
Memorial Hospital East Shiloh, Illinois Site Public Contact - (dschwab@wustl.edu)
Memorial Hospital North Colorado Springs, Colorado
Memorial Hospital West Pembroke Pines, Florida
Memorial Hospital of Carbondale Carbondale, Illinois Site Public Contact - (clinical.research@sih.net)
Memorial Medical Center Modesto, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Memorial Medical Center-Las Cruces Las Cruces, New Mexico Site Public Contact - (Deborah.Brown@LPNT.net)
Memorial Regional Hospital/Joe DiMaggio Children's Hospital Hollywood, Florida Site Public Contact - (OHR@mhs.net)
Mercy Cancer Center - Cape Girardeau Cape Girardeau, Missouri
Mercy Cancer Center - Carmichael Carmichael, California Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Mercy Cancer Center - Elk Grove Elk Grove, California Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Mercy Cancer Center - Rocklin Rocklin, California Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Mercy Cancer Center - Sacramento Sacramento, California Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Mercy Cancer Center-West Lakes Clive, Iowa
Mercy Clinic-Rolla-Cancer and Hematology Rolla, Missouri
Mercy Health - Perrysburg Hospital Perrysburg, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Health - Saint Anne Hospital Toledo, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Health - Saint Vincent Hospital Toledo, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Health Sylvania Radiation Oncology Center Toledo, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Hospital Coon Rapids, Minnesota
Mercy Hospital Coon Rapids, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Mercy Hospital Fort Smith Fort Smith, Arkansas
Mercy Hospital Joplin Joplin, Missouri Site Public Contact - (esmeralda.carrillo@mercy.net)
Mercy Hospital Oklahoma City Oklahoma City, Oklahoma
Mercy Hospital Saint Louis St Louis, Missouri
Mercy Hospital South St Louis, Missouri Site Public Contact - (Danielle.Werle@mercy.net)
Mercy Hospital Springfield Springfield, Missouri
Mercy Hospital Washington Washington, Missouri
Mercy Infusion Center - Chippewa St Louis, Missouri
Mercy Medical Center Rockville Centre, New York Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Mercy Medical Center - Des Moines Des Moines, Iowa
Mercy Medical Center-West Lakes West Des Moines, Iowa
Mercy Oncology and Hematology - Clayton-Clarkson Ballwin, Missouri
Mercy San Juan Medical Center Carmichael, California Site Public Contact - (OncologyResearch@DignityHealth.org)
Mercyhealth Hospital and Cancer Center - Janesville Janesville, Wisconsin Site Public Contact - (oncologyclinicaltrials@mhemail.org)
Methodist Medical Center of Illinois Peoria, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
MetroHealth Medical Center Cleveland, Ohio
Miami Valley Cancer Care and Infusion Greenville, Ohio
Miami Valley Hospital Dayton, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Miami Valley Hospital North Englewood, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Miami Valley Hospital South Centerville, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Michigan Healthcare Professionals Pontiac Pontiac, Michigan Site Public Contact - (Emily.Crofts@trinity-health.org)
Midlands Community Hospital Papillion, Nebraska
Mills Health Center San Mateo, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Mills-Peninsula Medical Center Burlingame, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Minnesota Oncology - Burnsville Burnsville, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Minnesota Oncology Hematology PA-Maplewood Maplewood, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Minnesota Oncology Hematology PA-Woodbury Woodbury, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Mission Hope Medical Oncology - Arroyo Grande Arroyo Grande, California Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Mission Hope Medical Oncology - Santa Maria Santa Maria, California Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Missouri Baptist Medical Center St Louis, Missouri
Missouri Baptist Sullivan Hospital Sullivan, Missouri
Mobile Infirmary Medical Center Mobile, Alabama
Moffitt Cancer Center Tampa, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Moffitt Cancer Center - McKinley Campus Tampa, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Moffitt Cancer Center at Wesley Chapel Wesley Chapel, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Moffitt Cancer Center-International Plaza Tampa, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Monmouth Medical Center Long Branch, New Jersey Site Public Contact - (mary.danish@rwjbh.org)
Monmouth Medical Center Southern Campus Lakewood, New Jersey
Montefiore Medical Center-Einstein Campus The Bronx, New York Site Public Contact - (eskwak@montefiore.org)
Monticello Cancer Center Monticello, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Morristown Medical Center Morristown, New Jersey
Mount Carmel East Hospital Columbus, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mount Carmel Grove City Hospital Grove City, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mount Carmel Health Center West Columbus, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mount Carmel New Albany Surgical Hospital New Albany, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mount Sinai Hospital New York, New York Site Public Contact - (CCTO@mssm.edu)
Mount Sinai Hospital Medical Center Chicago, Illinois Site Public Contact - (suhi@sinai.org)
Mount Sinai South Nassau Valley Stream, New York Site Public Contact - (surgical.oncology@snch.org)
Mount Sinai West New York, New York Site Public Contact - (CCTO@mssm.edu)
Munson Medical Center Traverse City, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
MyMichigan Medical Center Saginaw Saginaw, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
MyMichigan Medical Center Tawas Tawas City, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
NEA Baptist Memorial Hospital and Fowler Family Cancer Center - Jonesboro Jonesboro, Arkansas Site Public Contact - (Emily.Carvell@bmhcc.org)
NYP/Weill Cornell Medical Center New York, New York
NYU Langone Hospital - Long Island Mineola, New York
National Jewish Health-Western Hematology Oncology Golden, Colorado Site Public Contact - (glicht@co-cancerresearch.org)
Nebraska Cancer Specialists/Oncology Hematology West PC Grand Island, Nebraska
New Hampshire Oncology Hematology PA-Concord Concord, New Hampshire
New Ulm Medical Center New Ulm, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
New York-Presbyterian/Brooklyn Methodist Hospital Brooklyn, New York Site Public Contact - (Adg9003@nyp.org)
Newark Beth Israel Medical Center Newark, New Jersey Site Public Contact - (Christine.Kosmides@rwjbh.org)
Newark Radiation Oncology Newark, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Newland Medical Associates-Clarkston Clarkston, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Newland Medical Associates-Pontiac Pontiac, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Niagara Health System-Saint Catharines General Saint Catharines, Ontario
North Coast Cancer Care Sandusky, Ohio Site Public Contact - (TaussigResearch@ccf.org)
North Memorial Medical Health Center Robbinsdale, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
North Star Lodge Cancer Center at Yakima Valley Memorial Hospital Yakima, Washington Site Public Contact - (Memorial-ClinicalTrials@yvmh.org)
North York General Hospital Toronto, Ontario
NorthShore University HealthSystem-Evanston Hospital Evanston, Illinois
NorthShore University HealthSystem-Glenbrook Hospital Glenview, Illinois
NorthShore University HealthSystem-Highland Park Hospital Highland Park, Illinois
Northern Westchester Hospital Mount Kisco, New York Site Public Contact - (AMellor@northwell.edu)
Northside Hospital Atlanta, Georgia Site Public Contact - (ClinicalTrials@northside.com)
Northside Hospital - Duluth Duluth, Georgia Site Public Contact - (Clinical.trials@northside.com)
Northside Hospital - Gwinnett Lawrenceville, Georgia Site Public Contact - (Clinical.trials@northside.com)
Northwell Health Cancer Institute at Huntington Greenlawn, New York
Northwell Health/Center for Advanced Medicine Lake Success, New York
Northwest Cancer Center - Hobart Hobart, Indiana
Northwest Cancer Center - Main Campus Crown Point, Indiana
Northwest Cancer Center - Valparaiso Valparaiso, Indiana Site Public Contact - (CancerResearch@COMHS.org)
Northwest Oncology LLC Dyer, Indiana
Northwestern Medicine Cancer Center Delnor Geneva, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Cancer Center Kishwaukee DeKalb, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Cancer Center Warrenville Warrenville, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Glenview Outpatient Center Glenview, Illinois
Northwestern Medicine Grayslake Outpatient Center Grayslake, Illinois
Northwestern Medicine Lake Forest Hospital Lake Forest, Illinois Site Public Contact - (cancertrials@northwestern.edu)
Northwestern Medicine Orland Park Orland Park, Illinois Site Public Contact - (nctnprogram_rhlccc@northwestern.edu)
Northwestern University Chicago, Illinois Site Public Contact - (cancer@northwestern.edu)
Norton Audubon Hospital and Medical Campus Louisville, Kentucky
Norton Brownsboro Hospital and Medical Campus Louisville, Kentucky Site Public Contact - (Roster@nrgoncology.org)
Norton Hospital Pavilion and Medical Campus Louisville, Kentucky Site Public Contact - (cancerresearch@nortonhealthcare.org)
OSF Saint Anthony's Health Center Alton, Illinois
OSF Saint Francis Hospital and Medical Group Escanaba, Michigan Site Public Contact - (WI_research_admin@hshs.org)
Ochsner Hematology Oncology North Shore - Covington (West Region) Covington, Louisiana Site Public Contact - (Cheryl.kesler@ochsner.org)
Ochsner High Grove Baton Rouge, Louisiana Site Public Contact - (Camielle.beck@ochsner.org)
Ochsner Medical Center Jefferson New Orleans, Louisiana Site Public Contact - (Elisemarie.curry@ochsner.org)
Odette Cancer Centre- Sunnybrook Health Sciences Centre Toronto, Ontario
Ohio State University Comprehensive Cancer Center Columbus, Ohio Site Public Contact - (Jamesline@osumc.edu)
OhioHealth Mansfield Hospital Mansfield, Ohio
OhioHealth Marion General Hospital Marion, Ohio
Oklahoma Cancer Specialists and Research Institute-Tulsa Tulsa, Oklahoma
Oncology Associates at Mercy Medical Center Cedar Rapids, Iowa
Oncology Hematology Associates of Saginaw Valley PC Saginaw, Michigan
Oncology Hematology Care Inc-Kenwood Cincinnati, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
OptumCare Cancer Care at Charleston Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
OptumCare Cancer Care at Fort Apache Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
OptumCare Cancer Care at Seven Hills Henderson, Nevada Site Public Contact - (research@sncrf.org)
Orange Coast Memorial Medical Center Fountain Valley, California
Orion Cancer Care Findlay, Ohio
Orlando Health Cancer Institute Orlando, Florida Site Public Contact - (CancerClinicalTrials@orlandohealth.com)
Orlando Health Cancer Institute - Lake Mary Lake Mary, Florida Site Public Contact - (r-adultoncnewops@orlandohealth.com)
Ottawa Hospital and Cancer Center-General Campus Ottawa, Ontario
Our Lady of the Lake Physician Group Baton Rouge, Louisiana Site Public Contact - (research@ololrmc.com)
Overlook Hospital Summit, New Jersey
PCR Oncology Arroyo Grande, California Site Public Contact - (research@sncrf.org)
PROncology San Juan, Site Public Contact - (info@PRoncology.com)
Pacific Central Coast Health Center-San Luis Obispo San Luis Obispo, California Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Pali Momi Medical Center ‘Aiea, Hawaii
Palo Alto Medical Foundation Health Care Palo Alto, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Palo Alto Medical Foundation-Camino Division Mountain View, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Palo Alto Medical Foundation-Fremont Fremont, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Palo Alto Medical Foundation-Gynecologic Oncology Mountain View, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Palo Alto Medical Foundation-Santa Cruz Santa Cruz, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Palo Alto Medical Foundation-Sunnyvale Sunnyvale, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Pan American Center for Oncology Trials LLC San Juan, Site Public Contact - (ctsucontact@westat.com)
Pan American Center for Oncology Trials LLC San Juan, Site Public Contact - (marcia.cruzcorrea@panoncologytrials.com)
Pan American Center for Oncology Trials LLC - Cayey Cayey, Site Public Contact - (info@panoncologytrials.com)
Pan American Center for Oncology Trials LLC - Ciudadela San Juan, Site Public Contact - (info@panoncologytrials.com)
Pan American Center for Oncology Trials LLC - Dorado Dorado, Site Public Contact - (info@panoncologytrials.com)
Park Nicollet Clinic - Saint Louis Park Saint Louis Park, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Parkland Health Center - Farmington Farmington, Missouri
Parkland Memorial Hospital Dallas, Texas Site Public Contact - (canceranswerline@UTSouthwestern.edu)
Parkview Regional Medical Center Fort Wayne, Indiana
Peninsula Cancer Institute-Cancer Specialists of Tidewater Virginia Beach, Virginia Site Public Contact - (casey.morris@rivhs.com)
Peninsula Cancer Institute-Gloucester Gloucester, Virginia Site Public Contact - (casey.morris@rivhs.com)
Peninsula Cancer Institute-Newport News Newport News, Virginia Site Public Contact - (casey.morris@rivhs.com)
Peninsula Cancer Institute-Williamsburg Williamsburg, Virginia Site Public Contact - (casey.morris@rivhs.com)
Penn State Milton S Hershey Medical Center Hershey, Pennsylvania Site Public Contact - (CTO@hmc.psu.edu)
Pennsylvania Hospital Philadelphia, Pennsylvania
Penrose-Saint Francis Healthcare Colorado Springs, Colorado Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Phelps Health Delbert Day Cancer Institute Rolla, Missouri Site Public Contact - (research@phelpshealth.org)
Phelps Memorial Hospital Center Sleepy Hollow, New York
Phoebe Putney Memorial Hospital Albany, Georgia Site Public Contact - (ga_cares@augusta.edu)
Physicians' Clinic of Iowa PC Cedar Rapids, Iowa
Piedmont Fayette Hospital Fayetteville, Georgia
Piedmont Henry Hospital Stockbridge, Georgia
Piedmont Hospital Atlanta, Georgia
Piedmont Newnan Hospital Newnan, Georgia
Pocono Medical Center East Stroudsburg, Pennsylvania Site Public Contact - (Morgan_M.Horton@lvhn.org)
Poudre Valley Hospital Fort Collins, Colorado
Premier Blood and Cancer Center Dayton, Ohio
Presbyterian Kaseman Hospital Albuquerque, New Mexico Site Public Contact - (WBurman@phs.org)
Presbyterian Rust Medical Center/Jorgensen Cancer Center Rio Rancho, New Mexico Site Public Contact - (WBurman@phs.org)
Prisma Health Cancer Institute - Butternut Greenville, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Prisma Health Cancer Institute - Easley Easley, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Prisma Health Cancer Institute - Eastside Greenville, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Prisma Health Cancer Institute - Faris Greenville, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Prisma Health Cancer Institute - Greer Greer, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Prisma Health Cancer Institute - Seneca Seneca, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Prisma Health Cancer Institute - Spartanburg Boiling Springs, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
ProHealth D N Greenwald Center Mukwonago, Wisconsin Site Public Contact - (research.institute@phci.org)
ProHealth Oconomowoc Memorial Hospital Oconomowoc, Wisconsin
ProMedica Flower Hospital Sylvania, Ohio Site Public Contact - (PCIOncResearch@promedica.org)
ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital Toledo, Ohio Site Public Contact - (PCIOncResearch@promedica.org)
Providence Cancer Institute Clackamas Clinic Clackamas, Oregon
Providence Newberg Medical Center Newberg, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Providence Portland Medical Center Portland, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Providence Saint Vincent Medical Center Portland, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Providence Willamette Falls Medical Center Oregon City, Oregon Site Public Contact - (CanRsrchStudies@providence.org)
Queen's Cancer Cenrer - POB I Honolulu, Hawaii
Queen's Cancer Center - Kuakini Honolulu, Hawaii
Queen's Medical Center Honolulu, Hawaii
Queens Cancer Center Rego Park, New York
Rapid City Regional Hospital Rapid City, South Dakota Site Public Contact - (research@monument.health)
Reading Hospital West Reading, Pennsylvania
Reading Hospital McGlinn Cancer Institute at Phoenixville Phoenixville, Pennsylvania
Regions Hospital Saint Paul, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Reid Health Richmond, Indiana Site Public Contact - (clinical.trials@daytonncorp.org)
Renown Regional Medical Center Reno, Nevada Site Public Contact - (research@sncrf.org)
Rice Memorial Hospital Willmar, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Ridgeview Medical Center Waconia, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Ridley-Tree Cancer Center Santa Barbara, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Riverside Methodist Hospital Columbus, Ohio
Riverton Hospital Riverton, Utah Site Public Contact - (officeofresearch@imail.org)
Robert Wood Johnson University Hospital Somerset Somerville, New Jersey Site Public Contact - (Siby.Varughese@rwjbh.org)
Rochester General Hospital Rochester, New York Site Public Contact - (tia.derosa@rochestergeneral.org)
Rocky Mountain Cancer Centers-Longmont Longmont, Colorado Site Public Contact - (ResearchTracking@Centura.Org)
Rocky Mountain Cancer Centers-Penrose Colorado Springs, Colorado Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Roger Williams Medical Center Providence, Rhode Island Site Public Contact - (fdallesandro@chartercare.org)
Roper Hospital Charleston, South Carolina Site Public Contact - (Julia.Johnson@rsfh.com)
Royal Victoria Regional Health Centre Barrie, Ontario
Rush MD Anderson Cancer Center Chicago, Illinois Site Public Contact - (Cancer_Studies@rush.edu)
Rush MD Anderson Cancer Center at Rush Lisle Lisle, Illinois Site Public Contact - (Cancer_Studies@rush.edu)
Rush MD Anderson Cancer Center at Rush Oak Park Oak Park, Illinois Site Public Contact - (Cancer_Studies@rush.edu)
Rush-Copley Healthcare Center Yorkville, Illinois Site Public Contact - (Cancer.Research@rushcopley.com)
Rush-Copley Medical Center Aurora, Illinois Site Public Contact - (RCMC_Cancer_Research@rush.edu)
Rutgers Cancer Institute of New Jersey New Brunswick, New Jersey
Rutgers New Jersey Medical School Newark, New Jersey
SIH Cancer Institute Carterville, Illinois Site Public Contact - (clinical.research@sih.net)
SMC Center for Hematology Oncology Union Union, South Carolina Site Public Contact - (kmertz-rivera@gibbscc.org)
SSM Health Good Samaritan Mount Vernon, Illinois Site Public Contact - (gayla.hall@ssmhealth.com)
STCC at DHR Health Institute for Research and Development Edinburg, Texas Site Public Contact - (dhrresearch@dhr-rgv.com)
Saddleback Memorial Medical Center Laguna Hills, California
Saint Agnes Hospital Baltimore, Maryland
Saint Alphonsus Cancer Care Center-Boise Boise, Idaho Site Public Contact - (stephanie.couch@stjoeshealth.org)
Saint Alphonsus Cancer Care Center-Caldwell Caldwell, Idaho Site Public Contact - (stephanie.couch@stjoeshealth.org)
Saint Alphonsus Cancer Care Center-Nampa Nampa, Idaho Site Public Contact - (mccinfo@mtcancer.org)
Saint Alphonsus Cancer Care Center-Ontario Ontario, Oregon Site Public Contact - (mccinfo@mtcancer.org)
Saint Ann's Hospital Westerville, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Saint Anthony Hospital Lakewood, Colorado Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Saint Anthony Regional Hospital Carroll, Iowa Site Public Contact - (sbenson@iora.org)
Saint Barnabas Medical Center Livingston, New Jersey Site Public Contact - (joanne.loeb@rwjbh.org)
Saint Catherine Hospital Indianapolis, Indiana Site Public Contact - (Roster@nrgoncology.org)
Saint Clare Hospital Lakewood, Washington
Saint Elizabeth Boardman Hospital Boardman, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Saint Elizabeth Hospital Enumclaw, Washington
Saint Elizabeth Regional Medical Center Lincoln, Nebraska
Saint Elizabeth Youngstown Hospital Youngstown, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Saint Francis Cancer Center Greenville, South Carolina Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Saint Francis Hospital Federal Way, Washington
Saint Francis Medical Center Cape Girardeau, Missouri Site Public Contact - (sfmc@sfmc.net)
Saint Francis Regional Medical Center Shakopee, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Saint George Regional Medical Center St. George, Utah Site Public Contact - (officeofresearch@imail.org)
Saint John's Hospital - Healtheast Maplewood, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Saint Joseph Hospital - Cancer Centers of Colorado Denver, Colorado
Saint Joseph Hospital - Orange Orange, California
Saint Joseph Hospital East Lexington, Kentucky Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Saint Joseph London London, Kentucky Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Saint Joseph Radiation Oncology Resource Center Lexington, Kentucky Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Saint Joseph Regional Cancer Center Bryan, Texas
Saint Joseph Warren Hospital Warren, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Saint Luke's Cancer Institute - Boise Boise, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Cancer Institute - Fruitland Fruitland, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Cancer Institute - Meridian Meridian, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's Cancer Institute - Nampa Nampa, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Luke's East - Lee's Summit Lee's Summit, Missouri Site Public Contact - (aroland@kccop.org)
Saint Luke's Hospital of Kansas City Kansas City, Missouri Site Public Contact - (aroland@kccop.org)
Saint Luke's South Hospital Overland Park, Kansas Site Public Contact - (aroland@kccop.org)
Saint Mary Corwin Medical Center Pueblo, Colorado Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Saint Mary Medical Center Hobart, Indiana Site Public Contact - (CancerResearch@COMHS.org)
Saint Mary's Hospital and Regional Medical Center Grand Junction, Colorado Site Public Contact - (ccrp@co-cancerresearch.org)
Saint Mary's Oncology/Hematology Associates of Marlette Marlette, Michigan
Saint Mary's Oncology/Hematology Associates of West Branch West Branch, Michigan
Saint Mary's Regional Medical Center Reno, Nevada Site Public Contact - (research@sncrf.org)
Saint Michael Cancer Center Silverdale, Washington Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
Saint Michael's Hospital Toronto, Ontario
Saint Rita's Medical Center Lima, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Saint Vincent Frontier Cancer Center Billings, Montana
Saint Vincent Hospital Erie, Pennsylvania
Saint Vincent Hospital Cancer Center Green Bay Green Bay, Wisconsin Site Public Contact - (WI_research_admin@hshs.org)
Saint Vincent Hospital Cancer Center at Oconto Falls Oconto Falls, Wisconsin Site Public Contact - (WI_research_admin@hshs.org)
Saint Vincent Hospital Cancer Center at Saint Mary's Green Bay, Wisconsin Site Public Contact - (wi_research_admin@hshs.org)
Saint Vincent Hospital Cancer Center at Sturgeon Bay Sturgeon Bay, Wisconsin Site Public Contact - (wi_research_admin@hshs.org)
Sainte Genevieve County Memorial Hospital Sainte Genevieve, Missouri
Saints Mary and Elizabeth Hospital Louisville, Kentucky
Salinas Valley Memorial Salinas, California Site Public Contact - (tnielsen2@svmh.com)
San Juan City Hospital San Juan,
Sandra L Maxwell Cancer Center Cedar City, Utah Site Public Contact - (officeofresearch@imail.org)
Sanford Bismarck Medical Center Bismarck, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Broadway Medical Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Cancer Center Oncology Clinic Sioux Falls, South Dakota Site Public Contact - (OncologyClinicTrialsSF@sanfordhealth.org)
Sanford Cancer Center Worthington Worthington, Minnesota
Sanford Joe Lueken Cancer Center Bemidji, Minnesota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Roger Maris Cancer Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Thief River Falls Medical Center Thief River Falls, Minnesota
Sanford USD Medical Center - Sioux Falls Sioux Falls, South Dakota Site Public Contact - (OncologyClinicalTrialsSF@SanfordHealth.org)
Santa Cruz Radiation Oncology Medical Group Santa Cruz, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Saskatoon Cancer Centre Saskatoon, Saskatchewan
Scott and White Memorial Hospital Temple, Texas
Sechler Family Cancer Center Lebanon, Pennsylvania Site Public Contact - (doxenberg@wellspan.org)
Shaw Cancer Center Edwards, Colorado
Sheboygan Physicians Group Sheboygan, Wisconsin Site Public Contact - (wi_research_admin@hshs.org)
Sidney Kimmel Cancer Center Washington Township Sewell, New Jersey Site Public Contact - (ONCTrialNow@jefferson.edu)
Sinai Hospital of Baltimore Baltimore, Maryland
Siouxland Regional Cancer Center Sioux City, Iowa
Siteman Cancer Center at Christian Hospital St Louis, Missouri Site Public Contact - (info@siteman.wustl.edu)
Siteman Cancer Center at Saint Peters Hospital City of Saint Peters, Missouri Site Public Contact - (info@siteman.wustl.edu)
Siteman Cancer Center at West County Hospital Creve Coeur, Missouri Site Public Contact - (info@siteman.wustl.edu)
Siteman Cancer Center-South County St Louis, Missouri Site Public Contact - (info@siteman.wustl.edu)
Smilow Cancer Center/Yale-New Haven Hospital New Haven, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center - Guilford Guilford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center - Waterford Waterford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center - Westerly Westerly, Rhode Island Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Glastonbury Glastonbury, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Greenwich Greenwich, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Long Ridge Stamford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center at Saint Francis Hartford, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center-Fairfield Fairfield, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital Care Center-Trumbull Trumbull, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital-Derby Care Center Derby, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital-Orange Care Center Orange, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital-Torrington Care Center Torrington, Connecticut Site Public Contact - (canceranswers@yale.edu)
Smilow Cancer Hospital-Waterbury Care Center Waterbury, Connecticut Site Public Contact - (canceranswers@yale.edu)
Solinsky Center for Cancer Care Manchester, New Hampshire
South Jordan Health Center South Jordan, Utah Site Public Contact - (cancerinfo@hci.utah.edu)
South Pointe Hospital Warrensville Heights, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Southeastern Medical Oncology Center-Clinton Clinton, North Carolina Site Public Contact - (jfields@cancersmoc.com)
Southeastern Medical Oncology Center-Goldsboro Goldsboro, North Carolina Site Public Contact - (jfields@cancersmoc.com)
Southeastern Medical Oncology Center-Jacksonville Jacksonville, North Carolina Site Public Contact - (jfields@cancersmoc.com)
Southern Illinois University School of Medicine Springfield, Illinois
Southern Ohio Medical Center Portsmouth, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Spartanburg Medical Center Spartanburg, South Carolina Site Public Contact - (kmertz-rivera@gibbscc.org)
Springfield Clinic Springfield, Illinois
Springfield Memorial Hospital Springfield, Illinois Site Public Contact - (pallante.beth@mhsil.com)
Springfield Regional Cancer Center Springfield, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Springfield Regional Medical Center Springfield, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Staten Island University Hospital Staten Island, New York
Stony Brook University Medical Center Stony Brook, New York
Straub Clinic and Hospital Honolulu, Hawaii
Strecker Cancer Center-Belpre Belpre, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Stronach Regional Health Centre at Southlake Newmarket, Ontario
Summa Health Medina Medical Center Medina, Ohio Site Public Contact - (cancerresearch@summahealth.org)
Summa Health System - Akron Campus Akron, Ohio Site Public Contact - (cancerresearch@summahealth.org)
Summa Health System - Barberton Campus Barberton, Ohio Site Public Contact - (cancerresearch@summahealth.org)
Summit Health - Florham Park Campus Florham Park, New Jersey Site Public Contact - (mmackenzie@summithealth.com)
Summit Medical Group Berkeley Heights, New Jersey Site Public Contact - (Roster@nrgoncology.org)
Sutter Auburn Faith Hospital Auburn, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Sutter Cancer Centers Radiation Oncology Services-Auburn Auburn, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Sutter Cancer Centers Radiation Oncology Services-Cameron Park Cameron Park, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Sutter Cancer Centers Radiation Oncology Services-Roseville Roseville, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Sutter Cancer Research Consortium Novato, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Sutter Davis Hospital Davis, California Site Public Contact - (NCIclinicaltrials@sutterhealth.org)
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Using Nivolumab Alone or With Cabozantinib to Prevent Mucosal Melanoma Return After Surgery

ctrrecruit@vcu.edu

NCT05111574
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Inclusion Criteria:
* STEP 0 INCLUSION CRITERIA * Histologically proven mucosal melanoma by local pathology * Central PD-L1 tumor tissue submission * STEP 1 INCLUSION CRITERIA * Receipt of the central PD-L1 testing results available * Report is required for randomization of resection R0 or R1 patients * Testing must be started in Step 0 but results can be reported after registration for resection R2 patients * Disease status-Resected R0 or R1 disease patients. Patients eligible for randomization have resected R0 or R1 disease (with negative margins or positive microscopic margins) that must meet one of the following 4 criteria as defined below: * Regional lymph node (LN) involvement; OR * In-transit metastases/satellite primary disease; OR * Single localized, primary disease meeting one of the following site-specific requirements: * Head/neck - Sinonasal (including nasopharynx): any primary lesion; Nasal or oral cavity; pT4a or above, given slightly improved OS * NOTE: Conjunctival: does not meet the qualification for eligibility * Anorectal - any primary lesion * Vaginal/cervical - any primary, as they have 5 year OS rates of 5-25% * Urinary tract - any primary urethral or bladder tumor * Penile * Vulvar- American Joint Committee on Cancer (AJCC) cutaneous stage IIB or higher * Esophageal/gallbladder - any primary * Locoregionally recurrent following prior resection, meeting at least one of the above criteria * In addition, patients must have undergone cross-sectional imaging of the brain, chest, abdomen and pelvis with no evidence of distant metastatic disease * Disease status-Non-resected R2 or metastatic disease patients * Non-resected R2 or metastatic disease that is assessable and measurable radiographically or by physical examination * Prior Treatment: * No prior systemic checkpoint inhibitor therapy of mucosal melanoma, including in the adjuvant setting, is allowed. Prior adjuvant chemotherapy or interferon is allowed. * No other active, concurrent malignancy that requires ongoing systemic treatment or interferes with radiographic assessment of melanoma response as determined by the investigator. Exceptions may allow for adjuvant no evidence of disease (NED) cancers undergoing hormone based therapy may be eligible pending the other eligibility criteria are met and the principal investigator (PI) affirms the hormonal agent would not change the melanoma response. * Any radiation must have completed 28 days prior to randomization and the patient must have adequately recovered from its effects. * For resectable patients only: Surgery must have completed 28 days prior to randomization. * For resectable patients only: Surgery must have completed no more than 84 days prior to randomization. * Not pregnant and not nursing, because this study has an agent that has known genotoxic, mutagenic and teratogenic effects. Therefore, for women of childbearing potential only, a negative pregnancy test done =\< 7 days prior to registration is required * Age \>= 18 years * Eastern Cooperative Oncology Group (ECOG) performance status 0-2 * Absolute neutrophil count (ANC) \>= 1,500/mm\^3 * Platelet count \>= 100,000/mm\^3 * Creatinine =\< 1.5 x upper limit of normal (ULN) OR creatinine clearance (CrCl) \>= 50mL/min/1.73 m\^2 for patients with creatinine levels above institutional normal * Albumin \>= 2.8 g/dL * Total bilirubin =\< 1.5 x upper limit of normal (ULN) * Aspartate aminotransferase (AST)/alanine aminotransferase (ALT) =\< 2.5 x upper limit of normal (ULN) * No cardiovascular disease, including: * No history of acute coronary syndromes (including myocardial infarction and unstable angina), coronary artery bypass graft (CABG) coronary angioplasty, or stenting within 6 months prior to study entry. * No history of current class II or higher congestive heart failure as defined by the New York Heart Association (NYHA) functional classification system. * No refractory hypertension defined as a blood pressure of systolic \> 140 mmHg and/or diastolic \> 90 mmHg despite adequate attempts at anti-hypertensive therapy. * No history of myocarditis. * No history of syncope of cardiovascular etiology, uncontrolled cardiac arrhythmia, history of Mobitz II second degree or third degree heart block without a permanent pacemaker in Association (NYHA) class II to IV heart failure, or stroke/transient ischemic attack (TIA) within the past 3 months. * No corrected QT interval by Fridericia's formula (QTcF) \> 500 msec. Note: if initial QTcF is found to be \> 500 ms, two additional electrocardiograms (EKGs) separated by at least 3 minutes should be performed. If the average of these three consecutive results for QTcF is =\< 500 ms, the subject meets eligibility in this regard. * No underlying hematologic issues, including: * Congenital bleeding diathesis * Gastrointestinal (GI) bleeding requiring intervention within the past 6 months, unless directly related to mucosal melanoma * Active hemoptysis within 42 days prior to study enrollment. * Active tumor lesions with cavitations or tumor lesions which invade, encase, or abut major blood vessels. The anatomic location and characteristics of primary tumors or metastases as well as the medical history should be carefully reviewed in the selection of subjects for treatment with cabozantinib/placebo. * Pulmonary emboli or deep vein thromboses (DVT) that require an active anticoagulation regimen. * No known or suspected history of cytopenia (low white blood cell \[WBC\], hemoglobin or platelet count) of greater than 3 months duration with an unknown cause, myelodysplastic syndrome, or hematologic malignancies. * No clinical, laboratory or radiographic evidence of an active bacterial, fungal, or viral infection requiring treatment at the time of pre-registration (e.g., active symptoms of COVID-19 infection or a post-infectious symptomatic autoimmune syndrome, serious bacterial infections requiring antibiotics). * No known or suspected gastrointestinal disorder affecting absorption of oral medications. * Comorbid conditions: * No active autoimmune disease or any condition requiring systemic treatment with either corticosteroids (\> 10 mg daily of prednisone equivalents) or other immunosuppressive medications within 14 days of study drug administration. Inhaled or topical steroids and adrenal replacement doses \> 10 mg daily prednisone equivalents are permitted in the absence of active autoimmune disease. * No history of autoimmune motor neuropathy (e.g., Guillain-Barre syndrome, myasthenia gravis) or non-infectious pneumonitis. * No history of severe allergic reactions to an unknown allergen or any components of the study drugs or its excipients. * No history of gastrointestinal perforation or abdominal fistula. * No clinically suspected central nervous system (CNS) (leptomeningeal or parenchymal) metastases. Patients with a history of CNS metastasis(s) will be allowed as long as * The metastatic site(s) were adequately treated as demonstrated by clinical and radiographic improvement, AND * The patient has recovered from the intervention (no residual adverse events \> Common Terminology Criteria for Adverse Events \[CTCAE\] grade 1), AND * The patient has remained without occurrence of new or worsening CNS symptoms for a period of 28 days prior to enrollment. * No history of seizure or any condition that may increase the patient's seizure risk (e.g., prior cortical stroke, significant brain trauma) within 2 years. * No clinically active or chronic liver disease resulting in moderate/severe hepatic impairment (Child-Pugh class B or C), ascites, coagulopathy or bleeding due to liver dysfunction. * No untreated spinal cord compression or evidence of spinal metastases with a risk of impending fracture or spinal cord compression. Spinal metastases must have completed planned radiation or surgical therapy prior to registration. * Concomitant medications: * Chronic concomitant treatment with strong inhibitors of CYP3A4 is not allowed on this study. Patients on strong CYP3A4 inhibitors must discontinue the drug for 5 days prior to the start of study treatment. * Chronic concomitant treatment with strong CYP3A4 inducers is not allowed. Patients must discontinue the drug 5 days prior to the start of study treatment.
PROCEDURE: Biospecimen Collection, PROCEDURE: Bone Scan, DRUG: Cabozantinib S-malate, PROCEDURE: Computed Tomography, PROCEDURE: Echocardiography Test, PROCEDURE: Magnetic Resonance Imaging, BIOLOGICAL: Nivolumab, DRUG: Placebo Administration, PROCEDURE: Positron Emission Tomography
Anal Melanoma, Bladder Melanoma, Cervical Melanoma, Esophageal Melanoma, Gallbladder Melanoma, Head and Neck Mucosal Melanoma, Mucosal Melanoma, Nasopharyngeal Mucosal Melanoma, Oral Cavity Mucosal Melanoma, Penile Mucosal Melanoma, Rectal Melanoma, Recurrent Mucosal Melanoma, Sinonasal Mucosal Melanoma, Urethral Melanoma, Urinary System Mucosal Melanoma, Vaginal Melanoma, Vulvar Melanoma
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Abbott-Northwestern Hospital Minneapolis, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Alta Bates Summit Medical Center-Herrick Campus Berkeley, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Asplundh Cancer Pavilion Willow Grove, Pennsylvania
Atrium Medical Center-Middletown Regional Hospital Franklin, Ohio Site Public Contact - (clinical.trials@daytonncorp.org)
Avera Cancer Institute Sioux Falls, South Dakota Site Public Contact - (OncRegulatory@avera.org)
BJC Outpatient Center at Sunset Hills Sunset Hills, Missouri
Beacon Kalamazoo Cancer Center Kalamazoo, Michigan
Benefis Sletten Cancer Institute Great Falls, Montana Site Public Contact - (mccinfo@mtcancer.org)
Billings Clinic Cancer Center Billings, Montana Site Public Contact - (research@billingsclinic.org)
Bozeman Health Deaconess Hospital Bozeman, Montana Site Public Contact - (mccinfo@mtcancer.org)
Bronson Battle Creek Battle Creek, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Bronson Methodist Hospital Kalamazoo, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
California Pacific Medical Center-Pacific Campus San Francisco, California Site Public Contact - (clinicalresearch@sutterhealth.org)
Cancer Care Center of O'Fallon O'Fallon, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Care Specialists of Illinois - Decatur Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Centers of Southwest Oklahoma Research Lawton, Oklahoma
Cancer and Hematology Centers of Western Michigan - Norton Shores Norton Shores, Michigan Site Public Contact - (connie.szczepanek@crcwm.org)
Carle Cancer Center Urbana, Illinois Site Public Contact - (Research@carle.com)
Carle Physician Group-Effingham Effingham, Illinois Site Public Contact - (Research@carle.com)
Carle Physician Group-Mattoon/Charleston Mattoon, Illinois Site Public Contact - (Research@carle.com)
Carle at The Riverfront Danville, Illinois Site Public Contact - (Research@Carle.com)
Case Western Reserve University Cleveland, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
Centralia Oncology Clinic Centralia, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Community Hospital of Anaconda Anaconda, Montana Site Public Contact - (mccinfo@mtcancer.org)
Community Medical Center Missoula, Montana Site Public Contact - (mccinfo@mtcancer.org)
Corewell Health Grand Rapids Hospitals - Butterworth Hospital Grand Rapids, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health Lakeland Hospitals - Marie Yeager Cancer Center Saint Joseph, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Corewell Health Lakeland Hospitals - Niles Hospital Niles, Michigan
Corewell Health Reed City Hospital Reed City, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Crossroads Cancer Center Effingham, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Dana-Farber Cancer Institute Boston, Massachusetts
Dayton Physician LLC - Englewood Dayton, Ohio
Decatur Memorial Hospital Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Fairview Southdale Hospital Edina, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Good Samaritan Hospital - Cincinnati Cincinnati, Ohio Site Public Contact - (ResearchInstituteInquiries@CommonSpirit.org)
HSHS Sacred Heart Hospital Eau Claire, Wisconsin
Hematology Oncology Associates of CNY at Camillus Camillus, New York
Hematology Oncology Associates of Central New York-East Syracuse East Syracuse, New York
Jewish General Hospital Montreal, Quebec
Keck Medicine of USC Koreatown Los Angeles, California
Kettering Medical Center Kettering, Ohio
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Kootenai Health - Coeur d'Alene Coeur d'Alene, Idaho Site Public Contact - (mccinfo@mtcancer.org)
Laura and Isaac Perlmutter Cancer Center at NYU Langone New York, New York Site Public Contact - (CancerTrials@nyulangone.org)
Logan Health Medical Center Kalispell, Montana Site Public Contact - (mccinfo@mtcancer.org)
Los Angeles General Medical Center Los Angeles, California Site Public Contact - (uscnorrisinfo@med.usc.edu)
M D Anderson Cancer Center Houston, Texas Site Public Contact - (askmdanderson@mdanderson.org)
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Testing if High Dose Radiation Only to the Sites of Brain Cancer Compared to Whole Brain Radiation That Avoids the Hippocampus is Better at Preventing Loss of Memory and Thinking Ability

ctrrecruit@vcu.edu

NCT04804644
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Inclusion Criteria:
* Pathologically (histologically or cytologically) proven diagnosis of small cell lung cancer within 5 years of registration. If the original histologic proof of malignancy is greater than 5 years, then pathological (i.e., more recent) confirmation is required (e.g., from a systemic or brain metastasis); * Patients with de novo or recurrent small cell lung cancer are permitted. * Brain metastases =\< 4 cm in largest diameter and outside a 5-mm margin around either hippocampus must be visible on contrast-enhanced magnetic resonance imaging (MRI) performed =\< 21 days prior to study entry. * The total tumor volume must be 30 cm\^3 or less. Lesion volume will be approximated by measuring the lesion's three perpendicular diameters on contrast enhanced, T1-weighted MRI and the product of those diameters will be divided by 2 to estimate the lesion volume (e.g. xyz/2). Alternatively, direct volumetric measurements via slice by slice contouring on a treatment planning software package can be used to calculate the total tumor volume. * Brain metastases can be diagnosed synchronous to the initial diagnosis of small cell lung cancer or metachronous to the initial diagnosis and management of small cell lung cancer. * Brain metastases must be diagnosed on MRI, which will include the following elements: * REQUIRED MRI ELEMENTS * Post gadolinium contrast-enhanced T1-weighted three-dimensional (3D) spoiled gradient (SPGR). Acceptable 3D SPGR sequences include magnetization prepared 3D gradient recalled echo (GRE) rapid gradient echo (MP-RAGE), turbo field echo (TFE) MRI, BRAVO (Brain Volume Imaging) or 3D Fast FE (field echo). The T1-weighted 3D scan should use the smallest possible axial slice thickness, not to exceed 1.5 mm. * Pre-contrast T1 weighted imaging (3D imaging sequence strongly encouraged). * A minimum of one axial T2 FLAIR (preferred) or T2 sequence is required. This can be acquired as a two dimensional (2D) or 3D image. If 2D, the images should be obtained in the axial plane. * ADDITIONAL RECOMMENDATIONS * Recommendation is that an axial T2 FLAIR (preferred) sequence be performed instead of a T2 sequence. * Recommendation is that that pre-contrast 3D T1 be performed with the same parameters as the post-contrast 3D T1. * Recommendation is that imaging be performed on a 3 Tesla (3T) MRI. * Recommendation is that the study participants be scanned on the same MRI instrument at each time point. * Recommendation is that if additional sequences are obtained, these should meet the criteria outlined in Kaufmann et al., 2020. * If additional sequences are obtained, total imaging time should not exceed 60 minutes. * If additional metastases not known at the time of registration/randomization or seen in the MRI used for eligibility are subsequently found on the radiation therapy (RT) planning MRI such that the total intacranial volume exceeds 30 cm\^3, the patient is still considered eligible. * History/physical examination * Age \>= 18 * Karnofsky performance status of \>= 70 * Creatinine clearance \>= 30 ml/min * Following the diagnosis of brain metastases, patients can initiate and treat with systemic (chemotherapy and/or immunotherapy) before enrollment only if their brain metastases are asymptomatic and not located in eloquent locations (e.g., brainstem, pre-/post-central gyrus, visual cortex). However, within 21 days prior to enrollment, brain MRI must be repeated to confirm eligibility. * Patients with symptomatic brain metastases and/or brain metastases in eloquent locations (e.g., brainstem, pre-/post central gyrus, visual cortex) are eligible for enrollment on the trial; however, the specific treatment approach of starting with systemic therapy alone and delaying brain radiation is not recommended for these patients. * Concurrent immunotherapy with brain radiation (SRS or HA-WBRT) is permitted. * Negative urine or serum pregnancy test (in women of childbearing potential) within 14 days prior to registration. Women of childbearing potential and men who are sexually active must use contraception while on study. * Patients may have had prior intracranial surgical resection. * Because neurocognitive testing is the primary goal of this study, patients must be proficient in English or French Canadian. * The patient must provide study-specific informed consent prior to study entry. * Patients with impaired decision-making capacity are not permitted on study. * ELIGIBILITY CRITERIA PRIOR TO STEP 2 REGISTRATION * The following baseline neurocognitive tests must be completed within 21 days prior to Step 2 registration: HVLT-R, TMT, and COWA. The neurocognitive test will be uploaded into RAVE for evaluation by Dr. Wefel. Once the upload is complete, within 3 business days a notification will be sent via email to the RA to proceed to Step 2. * NOTE: Completed baseline neurocognitive tests can be uploaded at the time of Step 1 registration. * PRIOR TO STEP 2 REGISTRATION: The following baseline neurocognitive tests must be completed within 21 days prior to Step 2 registration: HVLT-R, TMT, and COWA. The neurocognitive tests will be uploaded into RAVE for evaluation by Dr. Wefel. Once the upload is complete, within 3 business days a notification will be sent via email to the RA to proceed to Step 2. NOTE: Completed baseline neurocognitive tests can be uploaded at the time of Step 1 registration.
Exclusion Criteria:
* Planned infusion of cytotoxic chemotherapy on the same day as SRS or HA-WBRT treatment. Patients may have had prior chemotherapy. Concurrent immunotherapy is permitted. * For patients receiving fractionated SRS on an every-other-day basis, planned infusion of cytotoxic chemotherapy is not permitted between SRS treatments. * Brainstem metastasis \> 10 cm\^3 * Prior allergic reaction to memantine. * Patients with definitive leptomeningeal metastases. * Known history of demyelinating disease such as multiple sclerosis. * Contraindication to MR imaging such as implanted metal devices that are MRI-incompatible, allergy to MRI contrast that cannot be adequately addressed with pre-contrast medications, or foreign bodies that preclude MRI imaging. (Questions regarding MRI compatibility of implanted objects should be reviewed with the Radiology Department performing the MRI). * Current use of (other N-methyl-D-aspartate \[NMDA\] antagonists) amantadine, ketamine, or dextromethorphan. * Radiographic evidence of hydrocephalus or other architectural change of the ventricular system resulting in significant anatomic distortion of the hippocampus, including placement of external ventricular drain or ventriculoperitoneal shunt. * Mild cases of hydrocephalus not resulting in significant anatomic distortion of the hippocampus are permitted. * Prior radiotherapy to the brain, including SRS, WBRT, or prophylactic cranial irradiation (PCI).
PROCEDURE: Biospecimen Collection, PROCEDURE: Magnetic Resonance Imaging, DRUG: Memantine Hydrochloride, OTHER: Neurocognitive Assessment, RADIATION: Stereotactic Radiosurgery, OTHER: Survey Administration, RADIATION: Whole-Brain Radiotherapy
Metastatic Lung Small Cell Carcinoma, Metastatic Malignant Neoplasm in the Brain, Recurrent Lung Small Cell Carcinoma, Stage IV Lung Cancer AJCC v8
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Location Contacts
Abbott-Northwestern Hospital Minneapolis, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Adams Cancer Center Gettysburg, Pennsylvania
Allan Blair Cancer Centre Regina, Saskatchewan
Allegheny General Hospital Pittsburgh, Pennsylvania
Aspirus Cancer Care - James Beck Cancer Center Rhinelander, Wisconsin Site Public Contact - (Beth.Knetter@aspirus.org)
Aspirus Cancer Care - Stevens Point Stevens Point, Wisconsin Site Public Contact - (Beth.Knetter@aspirus.org)
Aspirus Regional Cancer Center Wausau, Wisconsin
Avera Cancer Institute Sioux Falls, South Dakota
BJC Outpatient Center at Sunset Hills Sunset Hills, Missouri
Baptist Health Lexington Lexington, Kentucky
Beebe Health Campus Rehoboth Beach, Delaware
Beebe Medical Center Lewes, Delaware
Benefis Sletten Cancer Institute Great Falls, Montana
Billings Clinic Cancer Center Billings, Montana
Boston Medical Center Boston, Massachusetts
CHU de Quebec-L'Hotel-Dieu de Quebec (HDQ) Québec, Quebec
Cancer Care Center of O'Fallon O'Fallon, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Care Specialists of Illinois - Decatur Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Cancer Center of Western Wisconsin New Richmond, Wisconsin Site Public Contact - (mmcorc@healthpartners.com)
Carle Cancer Center Urbana, Illinois Site Public Contact - (Research@carle.com)
Carle Physician Group-Effingham Effingham, Illinois Site Public Contact - (Research@carle.com)
Carle Physician Group-Mattoon/Charleston Mattoon, Illinois Site Public Contact - (Research@carle.com)
Carle at The Riverfront Danville, Illinois Site Public Contact - (Research@Carle.com)
Carlisle Regional Cancer Center Carlisle, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
Caro Cancer Center Caro, Michigan
Case Western Reserve University Cleveland, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
Central Maryland Radiation Oncology in Howard County Columbia, Maryland
Centralia Oncology Clinic Centralia, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Chambersburg Hospital Chambersburg, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
Chelsea Hospital Chelsea, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Christiana Care Health System-Christiana Hospital Newark, Delaware
Christiana Care Health System-Concord Health Center Chadds Ford, Pennsylvania
Christiana Care Health System-Wilmington Hospital Wilmington, Delaware
Coborn Cancer Center at Saint Cloud Hospital Saint Cloud, Minnesota Site Public Contact - (coborncancercenter@centracare.com)
Cooper Hospital University Medical Center Camden, New Jersey
Crossroads Cancer Center Effingham, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Decatur Memorial Hospital Decatur, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Delaware Clinical and Laboratory Physicians PA Newark, Delaware
Delaware Health Center-Grady Cancer Center Delaware, Ohio
Divine Providence Hospital Williamsport, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
Drexel Town Square Health Center Oak Creek, Wisconsin
Emory Saint Joseph's Hospital Atlanta, Georgia
Emory University Hospital Midtown Atlanta, Georgia
Emory University Hospital/Winship Cancer Institute Atlanta, Georgia
Ephrata Cancer Center Ephrata, Pennsylvania
Fairview Clinics and Surgery Center Maple Grove Maple Grove, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Fairview Southdale Hospital Edina, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Freeman Health System Joplin, Montana Site Public Contact - (LJCrockett@freemanhealth.com)
Froedtert Menomonee Falls Hospital Menomonee Falls, Wisconsin
Froedtert West Bend Hospital/Kraemer Cancer Center West Bend, Wisconsin
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Geisinger Medical Oncology-Lewisburg Lewisburg, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Geisinger Wyoming Valley/Henry Cancer Center Wilkes-Barre, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Gibbs Cancer Center-Gaffney Gaffney, South Carolina
Gibbs Cancer Center-Pelham Greer, South Carolina
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Grant Medical Center Columbus, Ohio
Gundersen Lutheran Medical Center La Crosse, Wisconsin
HSHS Saint Elizabeth's Hospital O'Fallon, Illinois Site Public Contact - (morganthaler.jodi@mhsil.com)
Helen F Graham Cancer Center Newark, Delaware
IU Health Methodist Hospital Indianapolis, Indiana Site Public Contact - (iutrials@iu.edu)
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Indiana University/Melvin and Bren Simon Cancer Center Indianapolis, Indiana Site Public Contact - (iutrials@iu.edu)
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Kaiser Permanente Los Angeles Medical Center Los Angeles, California Site Public Contact - (clinical.trials@kp.org)
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Karmanos Cancer Institute at McLaren Greater Lansing Lansing, Michigan Site Public Contact - (ctoadmin@karmanos.org)
Lakeview Hospital Stillwater, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Langlade Hospital and Cancer Center Antigo, Wisconsin Site Public Contact - (Juli.Alford@aspirus.org)
Logan Health Medical Center Kalispell, Montana
Los Angeles General Medical Center Los Angeles, California Site Public Contact - (uscnorrisinfo@med.usc.edu)
Luminis Health Anne Arundel Medical Center Annapolis, Maryland
M D Anderson Cancer Center Houston, Texas Site Public Contact - (askmdanderson@mdanderson.org)
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MD Anderson in The Woodlands Conroe, Texas Site Public Contact - (askmdanderson@mdanderson.org)
Mary Bird Perkins Cancer Center Baton Rouge, Louisiana Site Public Contact - (clinicalresearch@marybird.com)
Mary Greeley Medical Center Ames, Iowa
Mayo Clinic Hospital in Arizona Phoenix, Arizona
McFarland Clinic - Ames Ames, Iowa Site Public Contact - (ksoder@mcfarlandclinic.com)
McLaren Cancer Institute-Bay City Bay City, Michigan Site Public Contact - (ctoadmin@karmanos.org)
McLaren Cancer Institute-Central Michigan Mount Pleasant, Michigan Site Public Contact - (ctoadmin@karmanos.org)
McLaren Cancer Institute-Flint Flint, Michigan Site Public Contact - (ctoadmin@karmanos.org)
McLaren Cancer Institute-Lapeer Region Lapeer, Michigan Site Public Contact - (ctoadmin@karmanos.org)
McLaren Cancer Institute-Macomb Mount Clemens, Michigan Site Public Contact - (ctoadmin@karmanos.org)
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McLeod Regional Medical Center Florence, South Carolina Site Public Contact - (dorie.sturgill@mcleodhealth.org)
MedStar Franklin Square Medical Center/Weinberg Cancer Institute Baltimore, Maryland
Medical College of Wisconsin Milwaukee, Wisconsin
Medical Oncology Hematology Consultants PA Newark, Delaware
Memorial Health University Medical Center Savannah, Georgia
Memorial Hospital North Colorado Springs, Colorado
Mercy Health - Perrysburg Hospital Perrysburg, Ohio Site Public Contact - (Jeffh@columbusccop.org)
Mercy Health - Saint Anne Hospital Toledo, Ohio
Mercy Hospital Coon Rapids, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Mercy Hospital Springfield Springfield, Missouri
Minnesota Oncology - Burnsville Burnsville, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
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Minnesota Oncology Hematology PA-Woodbury Woodbury, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Missouri Baptist Medical Center St Louis, Missouri
Missouri Baptist Sullivan Hospital Sullivan, Missouri
Moffitt Cancer Center Tampa, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Moffitt Cancer Center - McKinley Campus Tampa, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Moffitt Cancer Center at Wesley Chapel Wesley Chapel, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Moffitt Cancer Center-International Plaza Tampa, Florida Site Public Contact - (ClinicalTrials@moffitt.org)
Montefiore Medical Center - Moses Campus The Bronx, New York
Montefiore Medical Center-Einstein Campus The Bronx, New York
Montefiore Medical Center-Weiler Hospital The Bronx, New York
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MyMichigan Medical Center Saginaw Saginaw, Michigan
MyMichigan Medical Center Tawas Tawas City, Michigan
NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center New York, New York
Northern Westchester Hospital Mount Kisco, New York
Northside Hospital Atlanta, Georgia Site Public Contact - (ClinicalTrials@northside.com)
Northside Hospital-Cherokee Canton, Georgia Site Public Contact - (clinical.trials@northside.com)
Northside Hospital-Forsyth Cumming, Georgia Site Public Contact - (clinicaltrials@northside.com)
Northwell Health/Center for Advanced Medicine Lake Success, New York
Northwestern Medicine Cancer Center Delnor Geneva, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Cancer Center Kishwaukee DeKalb, Illinois Site Public Contact - (Donald.Smith3@nm.org)
Northwestern Medicine Cancer Center Warrenville Warrenville, Illinois Site Public Contact - (Donald.Smith3@nm.org)
OSF Saint Francis Medical Center Peoria, Illinois Site Public Contact - (andersonj@illinoiscancercare.com)
Ohio State University Comprehensive Cancer Center Columbus, Ohio Site Public Contact - (Jamesline@osumc.edu)
Oncology Hematology Associates of Saginaw Valley PC Saginaw, Michigan
Parkland Health Center - Farmington Farmington, Missouri
Regions Hospital Saint Paul, Minnesota Site Public Contact - (mmcorc@healthpartners.com)
Riverside Methodist Hospital Columbus, Ohio
Rush MD Anderson Cancer Center Chicago, Illinois
Rush-Copley Medical Center Aurora, Illinois Site Public Contact - (RCMC_Cancer_Research@rush.edu)
SMC Center for Hematology Oncology Union Union, South Carolina
Saint Francis Medical Center Cape Girardeau, Missouri Site Public Contact - (sfmc@sfmc.net)
Saint Luke's Cancer Center - Allentown Allentown, Pennsylvania
Saint Luke's Hospital - Monroe Campus Stroudsburg, Pennsylvania
Saint Luke's Hospital - Upper Bucks Campus Quakertown, Pennsylvania
Saint Luke's Hospital-Anderson Campus Easton, Pennsylvania
Saint Luke's Hospital-Quakertown Campus Quakertown, Pennsylvania
Saint Luke's University Hospital-Bethlehem Campus Bethlehem, Pennsylvania
Saint Mary's Oncology/Hematology Associates of Marlette Marlette, Michigan
Saint Mary's Oncology/Hematology Associates of West Branch West Branch, Michigan
Saint Vincent Hospital Erie, Pennsylvania
Sainte Genevieve County Memorial Hospital Sainte Genevieve, Missouri
Sands Cancer Center Canandaigua, New York
Sanford Bismarck Medical Center Bismarck, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Broadway Medical Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Cancer Center Oncology Clinic Sioux Falls, South Dakota Site Public Contact - (OncologyClinicTrialsSF@sanfordhealth.org)
Sanford Joe Lueken Cancer Center Bemidji, Minnesota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford Roger Maris Cancer Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford USD Medical Center - Sioux Falls Sioux Falls, South Dakota Site Public Contact - (OncologyClinicalTrialsSF@SanfordHealth.org)
Saskatoon Cancer Centre Saskatoon, Saskatchewan
Sechler Family Cancer Center Lebanon, Pennsylvania Site Public Contact - (doxenberg@wellspan.org)
Self Regional Healthcare Greenwood, South Carolina
Smilow Cancer Center/Yale-New Haven Hospital New Haven, Connecticut
Smilow Cancer Hospital Care Center - Guilford Guilford, Connecticut
Smilow Cancer Hospital Care Center - Waterford Waterford, Connecticut
Smilow Cancer Hospital Care Center at Greenwich Greenwich, Connecticut
Smilow Cancer Hospital Care Center-Trumbull Trumbull, Connecticut
Spartanburg Medical Center Spartanburg, South Carolina
State University of New York Upstate Medical University Syracuse, New York
The Carle Foundation Hospital Urbana, Illinois Site Public Contact - (Research@carle.com)
The James Graham Brown Cancer Center at University of Louisville Louisville, Kentucky
ThedaCare Regional Cancer Center Appleton, Wisconsin Site Public Contact - (ResearchDept@thedacare.org)
Thomas Jefferson University Hospital Philadelphia, Pennsylvania
TidalHealth Peninsula Regional Salisbury, Maryland
TidalHealth Richard A Henson Cancer Institute Ocean Pines, Maryland
Trinity Health IHA Medical Group Hematology Oncology - Brighton Brighton, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health IHA Medical Group Hematology Oncology - Canton Canton, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health IHA Medical Group Hematology Oncology - Chelsea Hospital Chelsea, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health IHA Medical Group Hematology Oncology Ann Arbor Campus Ypsilanti, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health Medical Center - Brighton Brighton, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health Medical Center - Canton Canton, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health Saint Joseph Mercy Hospital Ann Arbor Ann Arbor, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
Trinity Health Saint Mary Mercy Livonia Hospital Livonia, Michigan Site Public Contact - (MCRCwebsitecontactform@stjoeshealth.org)
UC Comprehensive Cancer Center at Silver Cross New Lenox, Illinois Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
UCHealth Memorial Hospital Central Colorado Springs, Colorado
UCHealth University of Colorado Hospital Aurora, Colorado
UF Health Cancer Institute - Gainesville Gainesville, Florida
UH Seidman Cancer Center at Lake Health Mentor Campus Mentor, Ohio Site Public Contact - (CTUReferral@UHhospitals.org)
UH Seidman Cancer Center at UH Avon Health Center Avon, Ohio
UM Baltimore Washington Medical Center/Tate Cancer Center Glen Burnie, Maryland
UM Sylvester Comprehensive Cancer Center at Coral Gables Coral Gables, Florida
UM Sylvester Comprehensive Cancer Center at Deerfield Beach Deerfield Beach, Florida
UM Upper Chesapeake Medical Center Bel Air, Maryland
UPMC Altoona Altoona, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
UPMC Cancer Center - Monroeville Monroeville, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
UPMC Cancer Center at UPMC Horizon Farrell, Pennsylvania Site Public Contact - (Roster@nrgoncology.org)
UPMC Cancer Centers - Arnold Palmer Pavilion Greensburg, Pennsylvania
UPMC Hillman Cancer Center Erie Erie, Pennsylvania Site Public Contact - (ClinicalResearchServices@upmc.edu)
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Yale University New Haven, Connecticut

A Study to Test the Addition of the Drug Cabozantinib to Chemotherapy in Patients With Newly Diagnosed Osteosarcoma

ctrrecruit@vcu.edu

NCT05691478
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Inclusion Criteria:
* Patients must be \< 40 years of age at the time of enrollment. * Patients must have a body surface area of \>= 0.8 m\^2 at the time of enrollment. * Patients must have histologic diagnosis (by institutional pathologist) of newly diagnosed high grade osteosarcoma. Primary tumors of all extremity and axial sites are eligible as long as diagnosis of high-grade osteosarcoma is established. Osteosarcoma as a second malignancy is eligible if no prior exposure to systemic chemotherapies. * Feasibility Phase (NOTE: as of Amendment #2B, the feasibility phase has been completed) Patients must have metastatic disease and a resectable primary tumor. Designation of a primary tumor as resectable will be determined at the time of diagnosis by the institutional multidisciplinary team. For this study, metastatic disease is defined as one or more of the following: * Lesions which are discontinuous from the primary tumor, are not regional lymph nodes, and do not share a bone or body cavity with the primary tumor. Skip lesions in the same bone as the primary tumor do not constitute metastatic disease. Skip lesions in an adjacent bone are considered bone metastases. * Lung metastases: defined as biopsy-proven metastasis or the presence of one or more pulmonary lesions \>= 5 mm, OR multiple pulmonary lesions \>= 3 mm or greater in size. * Bone metastases: Areas suspicious for bone metastasis based on fludeoxyglucose F-18 (18F-FDG)-positron emission tomography (PET) scan (or whole body technetium-99 bone scan if 18F-FDG-PET is unavailable at the treating institution) require confirmatory biopsy or supportive anatomic imaging of at least one suspicious site with either magnetic resonance imaging (MRI) or computed tomography (CT) (whole body 18F-FDG-PET/CT or 18F-FDG-PET/MR scans are acceptable). * Efficacy Phases (Phase 2/3) NOTE: as of Amendment #2B, the efficacy phase is open for enrollment. Patients with both localized and metastatic disease are eligible for the efficacy phase, regardless of resectability. Patients will be enrolled to two separate cohorts: * Cohort 1 (Standard Risk): Patients with non-pelvic primary osteosarcoma deemed to be resectable at the time of diagnosis by the institutional multidisciplinary team, without evidence of metastatic lesions. * Cohort 2 (High-Risk): Patients with a primary pelvic tumor, a primary tumor designated as unresectable by the institutional multidisciplinary team, AND/OR radiographic evidence of metastatic lesions. * A serum creatinine based on age/sex as follows (within 7 days prior to enrollment unless otherwise indicated): * (Age: Maximum Serum Creatinine \[mg/dL\]; Sex) * 1 month to \< 6 months: 0.4 (male); 0.4 (female) * 6 months to \< 1 year: 0.5 (male); 0.5 (female) * 1 to \< 2 years: 0.6 (male); 0.6 (female) * 2 to \< 6 years: 0.8 (male); 0.8 (female) * 6 to \< 10 years: 1 (male); 1 (female) * 10 to \< 13 years: 1.2 (male); 1.2 (female) * 13 to \< 16 years: 1.5 (male); 1.4 (female) * \>= 16 years: 1.7 (male); 1.4 (female) * OR - a 24 hour urine creatinine clearance \>= 70 mL/min/1.73 m\^2 * OR - a glomerular filtration rate (GFR) \>= 70 mL/min/1.73 m\^2. GFR must be performed using direct measurement with a nuclear blood sampling method OR direct small molecule clearance method (iothalamate or other molecule per institutional standard). * Note: Estimated GFR (eGFR) from serum creatinine, cystatin C or other estimates are not acceptable for determining eligibility. * Total bilirubin =\< 1.5 x upper limit of normal (ULN) for age (within 7 days prior to enrollment unless otherwise indicated) * Serum glutamate pyruvate transaminase (SGPT) (alanine aminotransferase \[ALT\]) =\< 135 U/L (within 7 days prior to enrollment unless otherwise indicated) * Note: For the purpose of this study, the ULN for SGPT (ALT) has been set to the value of 45 U/L * No history of congenital prolonged corrected QT (QTc) syndrome, New York Heart Association (NYHA) Class III or IV congestive heart failure, unstable angina pectoris, serious cardiac arrhythmias * Shortening fraction of \>= 27%, or * Ejection fraction of \>= 50% * Corrected QT interval by Fridericia (QTcF) \< 480 msec on electrocardiogram. Patients with Grade 1 prolonged QTc (450-480 msec) at time of study enrollment should have correctable causes of prolonged QTc addressed if possible (i.e., electrolytes, medications). * Peripheral absolute neutrophil count (ANC) \>= 1000/uL (within 7 days prior to enrollment unless otherwise indicated) * Platelet count \>= 100,000/uL (transfusion independent, defined as not receiving platelet transfusions within a 7-day period prior to enrollment) (within 7 days prior to enrollment unless otherwise indicated) * Hemoglobin \>= 8.0 g/dL (within 7 days prior to enrollment unless otherwise indicated) * International normalized ratio (INR) =\< 1.5 (within 7 days prior to enrollment unless otherwise indicated) * Human immunodeficiency virus (HIV)-infected patients on effective anti-retroviral therapy with undetectable viral load within 6 months are eligible as long as they are NOT receiving anti-retroviral agents that are strong inhibitors or inducers of CYP3A4, CYP2D6, and/or MRP2 transporter protein. * All patients and/or their parents or legal guardians must sign a written informed consent. * All institutional, Food and Drug Administration (FDA), and National Cancer Institute (NCI) requirements for human studies must be met.
Exclusion Criteria:
* Patients who have received previous systemic therapy for osteosarcoma or a prior oncologic diagnosis. * Patients who have central nervous system metastases. * Patients with central cavitating pulmonary lesions invading or encasing any major blood vessels in the lung. * Patients who are unable to swallow tablets. Tablets cannot be crushed or chewed. * Patients with gastrointestinal disorders including active disorders associated with a high risk of perforation or fistula formation. Specifically, no clinically significant gastrointestinal (GI) bleeding, GI perforation, bowel obstruction, intra-abdominal abscess or fistula for 6 months prior to enrollment, no hemoptysis or other signs of pulmonary hemorrhage for 3 months prior to enrollment. * Patients with active bleeding or bleeding diathesis. No clinically significant hematuria, hematemesis, or hemoptysis or other history of significant bleeding within 3 months prior to enrollment. * Patients with uncompensated or symptomatic hypothyroidism. Patients who have hypothyroidism controlled with thyroid replacement hormone are eligible. * Patients with moderate to severe hepatic impairment (Child-Pugh B or C). * Patients who have had primary tumor resection or attempted curative resection of metastases prior to enrollment. * Patients who have undergone other major surgical procedure (eg, laparotomy) within 14 days prior to enrollment. Thoracoscopic procedures for diagnostic purposes (biopsy of lung nodule) and central access such as port-a-cath placement are allowed. * Patients with a history of serious or non-healing wound or bone fracture (pathologic fracture of primary tumor is not considered exclusion). * Patients with any medical or surgical conditions that would interfere with gastrointestinal absorption of cabozantinib. * Patients with previously identify allergy or hypersensitivity to components of the study treatment formulations. * Patients who are receiving any other investigational agent not defined within this protocol are not eligible. * Patients who in the opinion of the investigator may not be able to comply with the safety monitoring requirements of the study are not eligible. * Patients who received enzyme-inducing anticonvulsants within 14 days prior to enrollment. * Patients with a prior history of hypertension (\> 95th percentile for age, height, and sex for patients \< 18 years and \> 140/90 mmHg for patients \>= 18 years requiring medication for blood pressure control. * Patients who are receiving drugs that prolong QTc. * Patients receiving anticoagulation with oral coumarin agents (eg warfarin), direct thrombin inhibitors (eg dabigatran), direct factor Xa inhibitor betrixaban, or platelet inhibitors (eg, clopidogrel). Low dose aspirin for cardioprotection (per local applicable guidelines) and low dose, low molecular weight heparins (LMWH) are permitted. Anticoagulation with therapeutic doses of LMWH and direct factor Xa inhibitors rivaroxaban or apixaban are allowed in subjects who are on a stable dose for at least 6 weeks before the first dose of study treatment, and who have had no complications from a thromboembolic event or the anticoagulation regimen. * Patients receiving strong CYP3A4 inducers or strong CYP3A4 inhibitors. * Female patients who are pregnant since fetal toxicities and teratogenic effects have been noted for several of the study drugs. A pregnancy test is required for female patients of childbearing potential. * Lactating females who plan to breastfeed their infants. * Sexually active patients of reproductive potential who have not agreed to use an effective contraceptive method for the duration of protocol therapy.
PROCEDURE: Bone Scan, DRUG: Cabozantinib S-malate, DRUG: Cisplatin, PROCEDURE: Computed Tomography, DRUG: Doxorubicin Hydrochloride, PROCEDURE: Magnetic Resonance Imaging, DRUG: Methotrexate, PROCEDURE: Surgical Procedure, PROCEDURE: X-Ray Imaging
High Grade Osteosarcoma, Localized Osteosarcoma, Metastatic Osteosarcoma, Secondary Osteosarcoma
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Study Locations

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Location Contacts
AdventHealth Orlando Apopka, Florida Site Public Contact - (FH.Cancer.Research@flhosp.org)
Albany Medical Center Albany, New York
Alberta Children's Hospital Calgary, Alberta Site Public Contact - (research4kids@ucalgary.ca)
Alfred I duPont Hospital for Children Wilmington, Delaware Site Public Contact - (Allison.bruce@nemours.org)
Allegiance Health Jackson, Michigan Site Public Contact - (CTOResearch@hfhs.org)
Alliance for Childhood Diseases/Cure 4 the Kids Foundation Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
Arkansas Children's Hospital Little Rock, Arkansas
Arnold Palmer Hospital for Children Orlando, Florida Site Public Contact - (Jennifer.spinelli@orlandohealth.com)
Augusta University Medical Center Augusta, Georgia Site Public Contact - (ga_cares@augusta.edu)
BI-LO Charities Children's Cancer Center Greenville, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
Banner Children's at Desert Mesa, Arizona
Banner University Medical Center - Tucson Tucson, Arizona Site Public Contact - (UACC-IIT@uacc.arizona.edu)
Baylor College of Medicine/Dan L Duncan Comprehensive Cancer Center Houston, Texas Site Public Contact - (burton@bcm.edu)
Blank Children's Hospital Des Moines, Iowa Site Public Contact - (samantha.mallory@unitypoint.org)
Bronson Methodist Hospital Kalamazoo, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
C S Mott Children's Hospital Ann Arbor, Michigan
CHU de Quebec-Centre Hospitalier de l'Universite Laval (CHUL) Québec, Site Public Contact - (rechclinique@crchudequebec.ulaval.ca)
CancerCare Manitoba Winnipeg, Manitoba Site Public Contact - (ctu_web@cancercare.mb.ca)
Cardinal Glennon Children's Medical Center St Louis, Missouri
Cedars Sinai Medical Center Los Angeles, California
Centre Hospitalier Universitaire Sainte-Justine Montreal, Quebec Site Public Contact - (yvan.samson@umontreal.ca)
Centre Hospitalier Universitaire de Sherbrooke-Fleurimont Sherbrooke, Quebec Site Public Contact - (crcinformation.chus@ssss.gouv.qc.ca)
Children's Healthcare of Atlanta - Arthur M Blank Hospital Atlanta, Georgia Site Public Contact - (Olivia.Floyd@choa.org)
Children's Hospital London, Ontario
Children's Hospital Colorado Aurora, Colorado Site Public Contact - (josh.b.gordon@nsmtp.kp.org)
Children's Hospital Los Angeles Los Angeles, California
Children's Hospital Medical Center Of Akron Akron, Ohio
Children's Hospital New Orleans New Orleans, Louisiana
Children's Hospital Of Eastern Ontario Ottawa, Ontario
Children's Hospital and Medical Center of Omaha Omaha, Nebraska
Children's Hospital of Alabama Birmingham, Alabama Site Public Contact - (oncologyresearch@peds.uab.edu)
Children's Hospital of Michigan Detroit, Michigan Site Public Contact - (helpdesk@childrensoncologygroup.org)
Children's Hospital of Orange County Orange, California Site Public Contact - (oncresearch@choc.org)
Children's Hospital of Philadelphia Philadelphia, Pennsylvania Site Public Contact - (CancerTrials@email.chop.edu)
Children's Hospital of Pittsburgh of UPMC Pittsburgh, Pennsylvania Site Public Contact - (jean.tersak@chp.edu)
Children's Hospital of San Antonio San Antonio, Texas Site Public Contact - (bridget.medina@christushealth.org)
Children's Hospital of Wisconsin Milwaukee, Wisconsin Site Public Contact - (MACCCTO@mcw.edu)
Children's Hospital of the King's Daughters Norfolk, Virginia Site Public Contact - (CCBDCresearch@chkd.org)
Children's Hospitals and Clinics of Minnesota - Minneapolis Minneapolis, Minnesota Site Public Contact - (pauline.mitby@childrensmn.org)
Children's Mercy Hospitals and Clinics Kansas City, Missouri Site Public Contact - (COGResearchGroup@cmh.edu)
Children's National Medical Center Washington D.C., District of Columbia Site Public Contact - (OncCRC_OnCall@childrensnational.org)
Christchurch Hospital Christchurch,
Cincinnati Children's Hospital Medical Center Cincinnati, Ohio Site Public Contact - (cancer@cchmc.org)
City of Hope Comprehensive Cancer Center Duarte, California Site Public Contact - (becomingapatient@coh.org)
Cleveland Clinic Foundation Cleveland, Ohio Site Public Contact - (TaussigResearch@ccf.org)
Connecticut Children's Medical Center Hartford, Connecticut
Cook Children's Medical Center Fort Worth, Texas Site Public Contact - (CookChildrensResearch@cookchildrens.org)
Corewell Health Children's Royal Oak, Michigan
Corewell Health Grand Rapids Hospitals - Helen DeVos Children's Hospital Grand Rapids, Michigan Site Public Contact - (crcwm-regulatory@crcwm.org)
Covenant Children's Hospital Lubbock, Texas Site Public Contact - (mbisbee@providence.org)
Dana-Farber Cancer Institute Boston, Massachusetts
Dartmouth Hitchcock Medical Center/Dartmouth Cancer Center Lebanon, New Hampshire Site Public Contact - (cancer.research.nurse@dartmouth.edu)
Dayton Children's Hospital Dayton, Ohio
Dell Children's Medical Center of Central Texas Austin, Texas Site Public Contact - (TXAUS-DL-SFCHemonc.research@ascension.org)
Driscoll Children's Hospital Corpus Christi, Texas Site Public Contact - (Crystal.DeLosSantos@dchstx.org)
Duke University Medical Center Durham, North Carolina
East Carolina University Greenville, North Carolina Site Public Contact - (eubankss@ecu.edu)
East Tennessee Childrens Hospital Knoxville, Tennessee
Eastern Maine Medical Center Bangor, Maine
El Paso Children's Hospital El Paso, Texas Site Public Contact - (ranjan.bista@ttuhsc.edu)
Geisinger Medical Center Danville, Pennsylvania Site Public Contact - (HemonCCTrials@geisinger.edu)
Golisano Children's Hospital of Southwest Florida Fort Myers, Florida Site Public Contact - (molly.arnstrom@leehealth.org)
Hackensack University Medical Center Hackensack, New Jersey
Henry Ford Cancer Institute-Downriver Brownstown, Michigan Site Public Contact - (CTOResearch@hfhs.org)
Henry Ford Hospital Detroit, Michigan Site Public Contact - (CTOResearch@hfhs.org)
Henry Ford Macomb Hospital-Clinton Township Clinton Township, Michigan Site Public Contact - (CTOResearch@hfhs.org)
Henry Ford Medical Center-Columbus Novi, Michigan Site Public Contact - (CTOResearch@hfhs.org)
Henry Ford Medical Center-Fairlane Dearborn, Michigan Site Public Contact - (CTOResearch@hfhs.org)
Henry Ford West Bloomfield Hospital West Bloomfield, Michigan Site Public Contact - (CTOResearch@hfhs.org)
Henry Ford Wyandotte Hospital Wyandotte, Michigan Site Public Contact - (nhay@hfhs.org)
Hospital for Sick Children Toronto, Ontario Site Public Contact - (ask.CRS@sickkids.ca)
IWK Health Centre Halifax, Nova Scotia Site Public Contact - (Research@iwk.nshealth.ca)
Jim Pattison Children's Hospital Saskatoon, Saskatchewan Site Public Contact - (Jessica.Marien@saskhealthauthority.ca)
Johns Hopkins All Children's Hospital St. Petersburg, Florida Site Public Contact - (Ashley.Repp@jhmi.edu)
Johns Hopkins University/Sidney Kimmel Cancer Center Baltimore, Maryland Site Public Contact - (jhcccro@jhmi.edu)
Kaiser Permanente Downey Medical Center Downey, California
Kaiser Permanente-Oakland Oakland, California Site Public Contact - (Kpoct@kp.org)
Kapiolani Medical Center for Women and Children Honolulu, Hawaii
Loma Linda University Medical Center Murrieta, California
Lucile Packard Children's Hospital Stanford University Palo Alto, California Site Public Contact - (ccto-office@stanford.edu)
Lurie Children's Hospital-Chicago Chicago, Illinois
M D Anderson Cancer Center Houston, Texas Site Public Contact - (askmdanderson@mdanderson.org)
Madigan Army Medical Center Tacoma, Washington Site Public Contact - (melissa.a.forouhar.mil@health.mil)
Maine Children's Cancer Program Scarborough, Maine Site Public Contact - (clinicalresearch@mainehealth.org)
Marshfield Medical Center-Marshfield Marshfield, Wisconsin Site Public Contact - (oncology.clinical.trials@marshfieldresearch.org)
Mary Bridge Children's Hospital and Health Center Tacoma, Washington Site Public Contact - (research@multicare.org)
Massachusetts General Hospital Cancer Center Boston, Massachusetts
Mattel Children's Hospital UCLA Los Angeles, California
Mayo Clinic in Rochester Rochester, Minnesota
MedStar Georgetown University Hospital Washington D.C., District of Columbia
Medical City Dallas Hospital Dallas, Texas
Memorial Health University Medical Center Savannah, Georgia Site Public Contact - (Lorraine.OHara@hcahealthcare.com)
Memorial Regional Hospital/Joe DiMaggio Children's Hospital Hollywood, Florida Site Public Contact - (OHR@mhs.net)
Memorial Sloan Kettering Cancer Center New York, New York
Mercy Hospital Saint Louis St Louis, Missouri
Methodist Children's Hospital of South Texas San Antonio, Texas Site Public Contact - (Vinod.GidvaniDiaz@hcahealthcare.com)
Miami Cancer Institute Miami, Florida
Miller Children's and Women's Hospital Long Beach Long Beach, California
Montefiore Medical Center - Moses Campus The Bronx, New York Site Public Contact - (eskwak@montefiore.org)
Morristown Medical Center Morristown, New Jersey
NYP/Columbia University Medical Center/Herbert Irving Comprehensive Cancer Center New York, New York Site Public Contact - (cancerclinicaltrials@cumc.columbia.edu)
NYP/Weill Cornell Medical Center New York, New York
NYU Langone Hospital - Long Island Mineola, New York Site Public Contact - (cancertrials@nyulangone.org)
Nationwide Children's Hospital Columbus, Ohio Site Public Contact - (Melinda.Triplet@nationwidechildrens.org)
Nemours Children's Clinic - Pensacola Pensacola, Florida Site Public Contact - (helpdesk@childrensoncologygroup.org)
Nemours Children's Clinic-Jacksonville Jacksonville, Florida Site Public Contact - (Allison.bruce@nemours.org)
Nemours Children's Hospital Orlando, Florida Site Public Contact - (Allison.bruce@nemours.org)
New York Medical College Valhalla, New York
Newark Beth Israel Medical Center Newark, New Jersey Site Public Contact - (Christine.Kosmides@rwjbh.org)
Nicklaus Children's Hospital Miami, Florida
Northwestern University Chicago, Illinois Site Public Contact - (cancer@northwestern.edu)
Norton Children's Hospital Louisville, Kentucky Site Public Contact - (CancerResource@nortonhealthcare.org)
Novant Health Presbyterian Medical Center Charlotte, North Carolina Site Public Contact - (kashah@novanthealth.org)
Ochsner Medical Center Jefferson New Orleans, Louisiana Site Public Contact - (Elisemarie.curry@ochsner.org)
Ohio State University Comprehensive Cancer Center Columbus, Ohio Site Public Contact - (Jamesline@osumc.edu)
Oregon Health and Science University Portland, Oregon Site Public Contact - (trials@ohsu.edu)
Penn State Children's Hospital Hershey, Pennsylvania
Perth Children's Hospital Perth, Western Australia Site Public Contact - (helpdesk@childrensoncologygroup.org)
Phoenix Childrens Hospital Phoenix, Arizona
Primary Children's Hospital Salt Lake City, Utah
Prisma Health Richland Hospital Columbia, South Carolina Site Public Contact - (Kim.Williams3@prismahealth.org)
ProMedica Toledo Hospital/Russell J Ebeid Children's Hospital Toledo, Ohio Site Public Contact - (PCIOncResearch@promedica.org)
Providence Sacred Heart Medical Center and Children's Hospital Spokane, Washington Site Public Contact - (HopeBeginsHere@providence.org)
Queensland Children's Hospital South Brisbane, Queensland
Rady Children's Hospital - San Diego San Diego, California
Rainbow Babies and Childrens Hospital Cleveland, Ohio
Riley Hospital for Children Indianapolis, Indiana
Rocky Mountain Hospital for Children-Presbyterian Saint Luke's Medical Center Denver, Colorado Site Public Contact - (PSGResearchSharedMailbox@HCAHealthcare.com)
Roswell Park Cancer Institute Buffalo, New York Site Public Contact - (askroswell@roswellpark.org)
Royal Children's Hospital Parkville, Victoria Site Public Contact - (Jordan.Hansford@rch.org.au)
Rutgers Cancer Institute of New Jersey-Robert Wood Johnson University Hospital New Brunswick, New Jersey
Saint Christopher's Hospital for Children Philadelphia, Pennsylvania
Saint Francis Cancer Center Greenville, South Carolina Site Public Contact - (Heather_Rich@bshsi.org)
Saint Francis Hospital Federal Way, Washington Site Public Contact - (Heather_Rich@bshsi.org)
Saint Joseph's Hospital/Children's Hospital-Tampa Tampa, Florida Site Public Contact - (jennifer.manns@baycare.org)
Saint Joseph's Regional Medical Center Paterson, New Jersey Site Public Contact - (HallL@sjhmc.org)
Saint Jude Children's Research Hospital Memphis, Tennessee Site Public Contact - (referralinfo@stjude.org)
Saint Jude Midwest Affiliate Peoria, Illinois
Saint Luke's Cancer Institute - Boise Boise, Idaho Site Public Contact - (eslinget@slhs.org)
Saint Vincent Hospital Cancer Center Green Bay Green Bay, Wisconsin Site Public Contact - (WI_research_admin@hshs.org)
Sanford Broadway Medical Center Fargo, North Dakota Site Public Contact - (OncologyClinicalTrialsFargo@sanfordhealth.org)
Sanford USD Medical Center - Sioux Falls Sioux Falls, South Dakota Site Public Contact - (OncologyClinicalTrialsSF@SanfordHealth.org)
Scott and White Memorial Hospital Temple, Texas
Seattle Children's Hospital Seattle, Washington
Sinai Hospital of Baltimore Baltimore, Maryland
Starship Children's Hospital Grafton, Auckland
State University of New York Upstate Medical University Syracuse, New York
Stony Brook University Medical Center Stony Brook, New York
Summerlin Hospital Medical Center Las Vegas, Nevada Site Public Contact - (research@sncrf.org)
Sydney Children's Hospital Randwick, New South Wales
The Children's Hospital at TriStar Centennial Nashville, Tennessee
The Children's Hospital at Westmead Westmead, New South Wales
The Montreal Children's Hospital of the MUHC Montreal, Quebec Site Public Contact - (info@thechildren.com)
The Steven and Alexandra Cohen Children's Medical Center of New York New Hyde Park, New York
Thomas Jefferson University Hospital Philadelphia, Pennsylvania Site Public Contact - (ONCTrialNow@jefferson.edu)
UCSF Benioff Children's Hospital Oakland Oakland, California Site Public Contact - (PedOncRschOAK@ucsf.edu)
UCSF Medical Center-Mission Bay San Francisco, California Site Public Contact - (cancertrials@ucsf.edu)
UF Health Cancer Institute - Gainesville Gainesville, Florida Site Public Contact - (cancer-center@ufl.edu)
UMC Cancer Center / UMC Health System Lubbock, Texas
UMass Memorial Medical Center - University Campus Worcester, Massachusetts Site Public Contact - (cancer.research@umassmed.edu)
UNC Lineberger Comprehensive Cancer Center Chapel Hill, North Carolina Site Public Contact - (cancerclinicaltrials@med.unc.edu)
UT Southwestern/Simmons Cancer Center-Dallas Dallas, Texas Site Public Contact - (canceranswerline@UTSouthwestern.edu)
University of Alberta Hospital Edmonton, Alberta Site Public Contact - (pedsoncologyresearch@ahs.ca)
University of California Davis Comprehensive Cancer Center Sacramento, California
University of Chicago Comprehensive Cancer Center Chicago, Illinois Site Public Contact - (cancerclinicaltrials@bsd.uchicago.edu)
University of Illinois Chicago, Illinois
University of Iowa/Holden Comprehensive Cancer Center Iowa City, Iowa
University of Kentucky/Markey Cancer Center Lexington, Kentucky
University of Maryland/Greenebaum Cancer Center Baltimore, Maryland
University of Miami Miller School of Medicine-Sylvester Cancer Center Miami, Florida
University of Michigan Rogel Cancer Center Ann Arbor, Michigan Site Public Contact - (CancerAnswerLine@med.umich.edu)
University of Minnesota/Masonic Cancer Center Minneapolis, Minnesota
University of Mississippi Medical Center Jackson, Mississippi
University of Missouri Children's Hospital Columbia, Missouri Site Public Contact - (snwq62@health.missouri.edu)
University of Nebraska Medical Center Omaha, Nebraska Site Public Contact - (unmcrsa@unmc.edu)
University of Oklahoma Health Sciences Center Oklahoma City, Oklahoma Site Public Contact - (ou-clinical-trials@ouhsc.edu)
University of Rochester Rochester, New York
University of Texas Health Science Center at San Antonio San Antonio, Texas Site Public Contact - (phoresearchoffice@uthscsa.edu)
University of Virginia Cancer Center Charlottesville, Virginia Site Public Contact - (uvacancertrials@hscmail.mcc.virginia.edu)
University of Wisconsin Carbone Cancer Center - University Hospital Madison, Wisconsin Site Public Contact - (clinicaltrials@cancer.wisc.edu)
VCU Massey Cancer Center at Stony Point Richmond, Virginia Site Public Contact - (ctoclinops@vcu.edu)
VCU Massey Comprehensive Cancer Center Richmond, Virginia Site Public Contact - (CTOclinops@vcu.edu)
Valley Children's Hospital Madera, California Site Public Contact - (Research@valleychildrens.org)
Vanderbilt University/Ingram Cancer Center Nashville, Tennessee
Wake Forest University Health Sciences Winston-Salem, North Carolina
Walter Reed National Military Medical Center Bethesda, Maryland
Washington University School of Medicine St Louis, Missouri Site Public Contact - (info@siteman.wustl.edu)
West Virginia University Charleston Division Charleston, West Virginia
Yale University New Haven, Connecticut Site Public Contact - (canceranswers@yale.edu)