drugset / Trial / NCT01571648

A Phase 1 Study to Evaluate the Pharmacokinetics and Tolerability of Oral Azacitidine in Japanese Patients With Myelodysplastic Syndromes

NCT01571648 ↗

Phase 1 Completed 5 enrolled Celgene Corporation
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the tolerability of oral azacitidine in the treatment of patients with Myelodysplastic Syndromes (MDS).

Timeline

Start
2012-04-01
Primary completion
2013-01-01
Completion
2013-01-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified 300 mg Oral