Study of Immunotherapy to Treat Advanced Prostate Cancer
Part of paid clinical trials in Mobile, Alabama.
- Sponsor
- Bristol-Myers Squibb
- Study ID
- NCT00861614
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- MALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ipilimumab — DRUG5 mg/ml solution, Intravenous, 10 mg/kg, Every 3 weeks for up to 4 doses in the Induction Phase. Every 12 weeks in the Maintenance Phase, Up to 24 weeks in Induction, 48+ weeks in the Maintenance Phase, or until Treatment Stopping Criteria are met, withdrawal of consent, lost to follow-up, death, study closure
- Placebo — DRUGSolution, Intravenous, 0 mg, Every 3 weeks for up to 4 doses in the Induction Phase. Every 12 weeks in the Maintenance Phase, up to 24 weeks in Induction, 48+ weeks in the Maintenance Phase, or until Treatment Stopping Criteria are met, withdrawal of consent, lost to follow-up, death, study closure
Study Details
The purpose of the study is to determine if advanced prostate cancer patients that are treated with radiotherapy (RT) plus ipilimumab live longer that those treated with RT alone
Key Dates
- Start date
- May 31, 2009
- Status verified
- Aug 2016
- Primary completion
- Nov 30, 2012
- Completion
- Aug 31, 2015
Study Design
- Enrollment
- 988 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Ipilimumab
- Placebo Comparator: Placebo
Primary Outcome Measure
Overall Survival (OS) [ Time Frame: Date of randomization to date of death ]
Locations (44)
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