drugset / Trial / NCT05209295

A Study to Evaluate CC-486/Onureg in Participants With Moderate or Severe Hepatic Impairment Compared With Normal Hepatic Function in Participants With Myeloid Malignancies

NCT05209295 ↗

Phase 1 Terminated 2 enrolled Bristol-Myers Squibb
Non-randomizedParallel-groupOpen-labelBasic science

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.

Timeline

Start
2024-07-12
Primary completion
2025-04-20
Completion
2025-04-20

Outcome

Outcome not reported

Stopped (Enrollment): “Insufficient Enrollment”

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified — Oral

Indications