Neoplasms Clinical Trial
Official title:
A Phase 1, Multicenter, Open-label Study to Evaluate the Pharmacokinetics of CC-486 (Onureg®) in Subjects With Moderate or Severe Hepatic Impairment Compared With Normal Hepatic Function in Adult Cancer Subjects
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.
n/a
| NCT number | NCT05209295 |
| Study type | Interventional |
| Source | Bristol-Myers Squibb |
| Contact | BMS Study Connect Contact Center www.BMSStudyConnect.com |
| Phone | 855-907-3286 |
| [email protected] | |
| Status | Not yet recruiting |
| Phase | Phase 1 |
| Start date | November 11, 2022 |
| Completion date | June 1, 2025 |
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