drugset / Trial / NCT00528983

Safety, Pharmacokinetics, and Pharmacodynamics of Oral Azacitidine in Subjects With Myelodysplastic Syndromes, Chronic Myelomonocytic Leukemia and Acute Myelogenous Leukemia

NCT00528983 ↗

Phase 1 Completed 133 enrolled Celgene Corporation
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether a tablet form of azacitidine that taken by mouth is safe. This Phase I study will also look at different doses and different treatment schedules in order to better understand the effects (positive and negative) of oral azacitidine on the body and on the disease MDS, AML and CMML.

Timeline

Start
2007-09-11
Primary completion
2013-07-31
Completion
2016-04-05

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified 75 mg Subcutaneous
Subject Azacitidine Other / unclassified 100 mg Subcutaneous
Subject Azacitidine Other / unclassified 120 mg Subcutaneous
Subject Azacitidine Other / unclassified 200 mg Subcutaneous
Subject Azacitidine Other / unclassified 300 mg Subcutaneous