drugset / Trial / NCT01305460

Intensified Azacitidine in High Risk Myelodysplastic Syndrome (MDS)

NCT01305460 ↗

Phase 1/2 Completed 27 enrolled Groupe Francophone des Myelodysplasies
NaSingle-groupOpen-labelTreatment

Summary

A phase I/II study of the efficacy and safety of an intensified schedule of Azacitidine (Vidaza®) in intermediate-2 and high risk MDS patients.

Timeline

Start
2011-07-05
Primary completion
2011-12
Completion
2015-11-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Azacitidine Other / unclassified 75 mg/m2 —