drugset / Trial / NCT00282399

A Clinical Trial of Decitabine in Patients With Myelodysplastic Syndrome

NCT00282399 ↗

Phase 1 Terminated 41 enrolled Eisai Inc.
RandomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study was to determine which of the doses of decitabine maximizes genomic demethylation in patients with Myelodysplastic Syndrome (MDS).

Timeline

Start
2006-10
Primary completion
2008-10
Completion
2009-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Decitabine Small molecule 2 mg/m2 Subcutaneous
Subject Decitabine Small molecule 5 mg/m2 Subcutaneous
Subject Decitabine Small molecule 10 mg/m2 Subcutaneous