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Clinical Trial Summary

The purpose of this study is to evaluate the effect of moderate and severe liver impairment on the drug levels of oral azacitidine and the safety and tolerability of oral azacitidine in adult cancer participants. This study will also evaluate the safety and tolerability of intravenous/subcutaneous azacitidine in adult cancer participants.

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 Not yet recruiting
Phase Phase 1
Start date November 11, 2022
Completion date June 1, 2025

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