BMS-936558 (MDX-1106) In Subjects With Advanced/Metastatic Clear-Cell Renal Cell Carcinoma (RCC)
Part of paid clinical trials in La Jolla, California.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT01354431
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- nivolumab — BIOLOGICALSolution, Intravenous (IV), 0.3 mg/kg, every 3 weeks (Q 3 weeks), Until Progressive disease (PD), toxicity or discontinue for other reasons
- nivolumab — BIOLOGICALSolution, Intravenous (IV), 2.0 mg/kg, every 3 weeks (Q 3 weeks), Until Progressive disease (PD), toxicity or discontinue for other reasons
- nivolumab — BIOLOGICALSolution, Intravenous (IV), 10.0 mg/kg, every 3 weeks (Q 3 weeks), Until Progressive disease (PD), toxicity or discontinue for other reasons
Study Details
The purpose of this study is to measure how active BMS-936558 (nivolumab) is against Renal Cell Carcinoma (RCC) as measured by the disease not progressing and whether a dose response relationship exists.
Key Dates
- Start date
- May 31, 2011
- Status verified
- May 2022
- Primary completion
- May 15, 2013
- Completion
- Apr 15, 2021
Study Design
- Enrollment
- 168 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm 1: nivolumab - 0.3 mg/kg
- Experimental: Arm 2: nivolumab - 2.0 mg/kg
- Experimental: Arm 3: nivolumab - 10.0 mg/kg
Primary Outcome Measure
Progression Free Survival (PFS) [ Time Frame: From randomization to disease progression or death (up to approximately 2 years) ]
Locations (34)
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