drugset / Trial / NCT01011283

To Demonstrate Superiority of Decitabine Over Azacitidine in Subjects With Intermediate- or High-risk MDS.

NCT01011283

Phase 4 Terminated 26 enrolled Eisai Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the response of patients with Intermediate or High Risk myelodysplastic syndromes (MDS) following treatment with decitabine or azacitidine.

Timeline

Start
2009-11
Primary completion
2011-01
Completion

Drugs

EvaluationDrugModalityDoseRoute
Comparator Azacitidine Other / unclassified 75 mg/m2 Subcutaneous
Comparator Decitabine Small molecule 20 mg/m2 Intravenous