Safety and Efficacy Study of BMS-908662 in Combination With Ipilimumab in Subjects With Advanced Melanoma
Completed · Phase 1
Conditions studied: Melanoma
In brief
The purpose of the study is to identify a safe and tolerable dose of BMS-908662 in combination with ipilimumab; and then to evaluate the anti-tumor response to BMS-908662 when administered in combination with ipilimumab.
Key facts
- Study ID
- NCT01245556
- Run by
- Bristol-Myers Squibb
- People needed
- 8
- Starts
- 2011-01-01
- Expected to finish
- 2012-11-01
- Last updated by the study team
- 2013-06-12
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
Where it is running
- H. Lee Moffitt Cancer Center & Research Institute — Tampa, Florida, United States
- Jedd D. Wolchok, Md,Phd — New York, New York, United States
Full record on ClinicalTrials.gov
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