A Phase II Study Of Nivolumab/ Bevacizumab/Rucaparib
Part of paid clinical trials in Boston, Massachusetts.
- Sponsor
- Dana-Farber Cancer Institute
- Study ID
- NCT02873962
- Phase
- PHASE2
- Status
- Active Not Recruiting
Conditions
- Fallopian Tube Cancer
- Ovarian Cancer
- Peritoneal Cancer
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Bevacizumab — DRUG* Bevacizumab will be given intravenously at a pre-determined dosage * One dose reduction will be allowed for Bevacizumab
- Nivolumab — DRUG* Nivolumab injection is to be administered as an IV infusion at a pre-determined dosage. * No dose reductions or escalations will be allowed for Nivolumab
- Rucaparib — DRUG* Rucaparib will be taken orally twice daily on days 1-14 at a pre-determined dosage. * Up to three dose reductions will be allowed for Rucaparib (depending on cohort).
Study Details
This research study is evaluating three drugs called Nivolumab, Bevacizumab, and Rucaparib as a possible treatment for relapsed Relapsed Ovarian, Fallopian Tube Or Peritoneal Cancer.
Key Dates
- Start date
- Nov 10, 2016
- Status verified
- Mar 2026
- Primary completion
- Feb 28, 2025
- Completion
- Jan 31, 2027
Study Design
- Enrollment
- 72 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort 1: Nivolumab with BevacizumabPatients will receive treatment every 14 days with Nivolumab and Bevacizumab administered on day 1 of each cycle.
- Experimental: Cohort 2: Nivolumab with Bevacizumab and RucaparibPatients will receive treatment every 14 days with Nivolumab, Bevacizumab administered on day 1 of each cycle and Rucaparib will be taken orally twice daily on days 1-14 .
- Experimental: Cohort 3: Nivolumab with Bevacizumab and RucaparibPatients will receive treatment every 14 days with Nivolumab, Bevacizumab administered on day 1 of each cycle and Rucaparib will be taken orally twice daily on days 1-14 .
Primary Outcome Measure
Cohort 1: Objective Response Rate [ Time Frame: 18 months ]
Locations (3)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Beth Israel Deaconess Medical Center | Boston | Massachusetts | 02215 | - |
| Dana Farber Cancer Institute | Boston | Massachusetts | 02115 | - |
| Massachusetts General Hospital | Boston | Massachusetts | 02114 | - |
Related coverage on Hipa.ai
- Nivolumab Trial Results Posted for Ovarian, Fallopian Tube, Peritoneal CancerNivolumab · Apr 1, 2026 · ClinicalTrials.gov
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