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Clinical Trial Summary

The main purpose of this study is to characterize the safety, tolerability, dose limiting toxicities, best route of administration, maximum tolerated dose, maximum administered dose, or alternative dose of BMS-986301 alone or in combination with nivolumab and ipilimumab in participants with cancers that have failed to respond to T cell checkpoint inhibiting antibodies.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03956680
Study type Interventional
Source Bristol-Myers Squibb
Contact
Status Completed
Phase Phase 1
Start date March 26, 2019
Completion date April 17, 2024

See also
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