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Clinical Trial Summary

The primary purpose of this study is to evaluate the safety and effectiveness of daily doses of BMS-986115 in subjects with advanced solid tumors


Clinical Trial Description

n/a


Study Design

Allocation: Non-Randomized, Endpoint Classification: Safety Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT01986218
Study type Interventional
Source Bristol-Myers Squibb
Contact
Status Terminated
Phase Phase 1
Start date November 2013
Completion date March 2016

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