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Clinical Trial Summary

The purpose of this study is to assess the safety, tolerability, drug levels, drug efficacy and determine the recommended dose of BMS-986497 in participants with relapsed or refractory acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06419634
Study type Interventional
Source Bristol-Myers Squibb
Contact BMS Study Connect Contact Center www.BMSStudyConnect.com
Phone 855-907-3286
Email Clinical.Trials@bms.com
Status Not yet recruiting
Phase Phase 1
Start date May 30, 2024
Completion date September 16, 2030

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