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Clinical Trial Summary

The purpose of this study is to evaluate the effect of moderate or severe liver impairment on the drug levels of oral azacitidine and the safety and tolerability of oral azacitidine in participants with myeloid malignancies.

Clinical Trial Description


Study Design

Related Conditions & MeSH terms

NCT number NCT05209295
Study type Interventional
Source Bristol-Myers Squibb
Contact BMS Study Connect Contact Center
Phone 855-907-3286
Status Recruiting
Phase Phase 1
Start date July 31, 2024
Completion date June 1, 2025

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