A Study to Test Combination Treatments in People With Advanced Renal Cell Carcinoma
Part of paid clinical trials in New Haven, Connecticut.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT02996110
- Phase
- PHASE2
- Status
- Completed
Conditions
- Advanced Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Nivolumab — BIOLOGICALSpecified Dose on Specified Days
- Ipilimumab — BIOLOGICALSpecified Dose on Specified Days
- Relatlimab — BIOLOGICALSpecified Dose on Specified Days
- BMS-986205 — DRUGSpecified Dose on Specified Days
- BMS-813160 — DRUGSpecified Dose on Specified Days
Study Details
The purpose of this study is to test the effectiveness and safety of various nivolumab combinations compared to nivolumab and ipilimumab in participants with advanced kidney cancer
Key Dates
- Start date
- Feb 2, 2017
- Status verified
- Nov 2022
- Primary completion
- Nov 23, 2021
- Completion
- Nov 23, 2021
Study Design
- Enrollment
- 182 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Nivolumab + IpilimumabNivolumab + Ipilimumab
- Experimental: Nivolumab + RelatlimabNivolumab + Relatlimab
- Experimental: Nivolumab + BMS-986205Nivolumab + BMS-986205
- Experimental: Nivolumab + BMS-813160Nivolumab + BMS-813160 (CCR2/5 dual antagonist)
Primary Outcome Measure
Objective Response Rate (ORR) Per Investigator [ Time Frame: From first dose of study treatment until progression or subsequent anticancer therapy, whichever occurs first (assessed up to approximately 247 weeks) ]
Locations (20)
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