A Study in Ovarian Cancer Patients Evaluating Rucaparib and Nivolumab as Maintenance Treatment Following Response to Front-Line Platinum-Based Chemotherapy
RucaparibNivolumabPlacebo Oral TabletPlacebo IV Infusion
Rucaparib: Oral rucaparib will be administered twice daily
Nivolumab: IV nivolumab will be administered once every 4 weeks
Placebo Oral Tablet: Placebo tablets will be administered twice daily
Placebo IV Infusion: IV placebo will be administered once every 4 weeks
Study summary
This is a Phase 3, randomized, multinational, double-blind, dual placebo-controlled, 4-arm study evaluating rucaparib and nivolumab as maintenance treatment following response to front-line treatment in newly diagnosed ovarian cancer patients. Response to treatment will be analyzed based on homologous recombination (HR) status of tumor samples.
Eligibility
Sex
FEMALE
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Newly diagnosed advanced (FIGO stage III-IV) epithelial ovarian, fallopian tube, or primary peritoneal cancer.
* Completed cytoreductive surgery, including at least a bilateral salpingo-oophorectomy and partial omentectomy, either prior to chemotherapy (primary surgery) or following neoadjuvant chemotherapy (interval debulking)
* Completed first-line platinum-based chemotherapy and surgery with a response, in the opinion of the Investigator
* Sufficient tumor tissue for planned analysis
* ECOG performance status of 0 or 1
* Patients must be 20 years of age to consent in Japan, Taiwan and South Korea; in all other participating countries patients must be 18 years of age to consent
Exclusion Criteria:
* Pure sarcomas or borderline tumors or mucinous tumors
* Active second malignancy
* Known central nervous system brain metastases
* Any prior treatment for ovarian cancer, other than the first-line platinum regimen
* Evidence of interstitial lung disease or active pneumonitis
* Active, known or suspected autoimmune disease
* Condition requiring active systemic treatment with either corticosteroids (\>10 mg daily prednisone equivalent) or other immunosuppressive medications
Primary outcome measure(s)
Monotherapy Arm B and Arm D: Investigator Assessed Progression-free Survival (PFS) — From randomization until disease progression (up to the primary data analysis at approximately 39 months) PFS by investigator was defined as the time from randomization to disease progression, according to Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1 as assessed by the investigator, or death due to any cause, whichever occurred first.
Progressive disease was defined as a 20% increase in the sum of the longest diameter of measurable lesions, an unequivocal increase in existing non-measurable lesion(s), or the appearance of unequivocal new lesion(s).
Monotherapy Arm B and Arm D: Investigator Assessed PFS — From randomization until disease progression (up to the primary data analysis at approximately 39 months) PFS by investigator was defined as the time from randomization to disease progression, according to RECIST v1.1 as assessed by the investigator, or death due to any cause, whichever occurred first.
Progressive disease was defined as a 20% increase in the sum of the longest diameter of measurable lesions, an unequivocal increase in existing non-measurable lesion(s), or the appearance of unequivocal new lesion(s).
Combination Therapy Arm A and Arm B: Investigator Assessed PFS — From randomization until disease progression (up to the combination therapy interim analysis at approximately 66 months) PFS by investigator was defined as the time from randomization to disease progression, according to RECIST v1.1 as assessed by the investigator, or death due to any cause, whichever occurred first.
Progressive disease was defined as a 20% increase in the sum of the longest diameter of measurable lesions, an unequivocal increase in existing non-measurable lesion(s), or the appearance of unequivocal new lesion(s).
Trial sites (238)
Facility
City
Region
Status
Arizona Oncology Associates, PC - HAL
Phoenix
Arizona
Arizona Oncology Associates, PC - HOPE
Tucson
Arizona
The University of Arizona Cancer Center
Tucson
Arizona
John Muir Clinical Research Center
Concord
California
UCLA Women's Health Clinical Research Unit
Los Angeles
California
Kaiser Permanente Northern California
San Francisco
California
University of Colorado Cancer Center
Aurora
Colorado
Rocky Mountain Cancer Centers
Lakewood
Colorado
Yale University
New Haven
Connecticut
Florida Gynecologic Oncology
Fort Myers
Florida
MD Anderson Cancer Center-Baptist
Jacksonville
Florida
Baptist Health Medical Group Oncology, LLC
Miami
Florida
Florida Hospital
Orlando
Florida
Northside Hospital
Atlanta
Georgia
Augusta University
Augusta
Georgia
Rush University Medical Center
Chicago
Illinois
Dr. Sudarshan K. Sharma, Ltd - Gynecologic Oncology
Hinsdale
Illinois
Ferrell-Duncan Clinic
Springfield
Illinois
Community Health Network
Indianapolis
Indiana
University of Iowa Hospitals
Iowa City
Iowa
University of Kansas Cancer Center
Westwood
Kansas
University of Kentucky
Lexington
Kentucky
Norton Cancer Institute
Louisville
Kentucky
Ochsner Medical Center
New Orleans
Louisiana
Maine Medical Center
Scarborough
Maine
SKCCC at Johns Hopkins
Baltimore
Maryland
Massachusetts General Hospital
Boston
Massachusetts
Karmanos Cancer Institute
Detroit
Michigan
Metro Minnesota Community Oncology Research Consortium
Saint Louis Park
Minnesota
Washington University School of Medicine
St Louis
Missouri
Women's Cancer Center of Nevada
Las Vegas
Nevada
MD Anderson Cancer Center at Cooper
Camden
New Jersey
Summit Medical Group
Florham Park
New Jersey
Women's Cancer Care Associates
Albany
New York
Broome Oncology, LLC
Johnson City
New York
Northwell Health Monter Cancer Center
Lake Success
New York
New York University Medical Center
New York
New York
University of North Carolina
Chapel Hill
North Carolina
University of Cincinnati
Cincinnati
Ohio
Oncology Hematology Care, Inc
Cincinnati
Ohio
+ 198 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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