drugset / Trial / NCT00828802

Lenalidomide and Decitabine in High Grade Myelodysplastic Syndromes

NCT00828802 ↗

Phase 1 Completed 15 enrolled Duke University Celgene Corporation · collab
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to find out what dose of lenalidomide is safe to use in combination with decitabine when given in people with myelodysplastic syndrome.

Timeline

Start
2009-03
Primary completion
2012-08
Completion
2012-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Decitabine Small molecule 20 mg/m2 Intravenous
Subject Lenalidomide Other / unclassified 5 mg —
Subject Lenalidomide Other / unclassified 10 mg —
Subject Lenalidomide Other / unclassified 15 mg —
Subject Lenalidomide Other / unclassified 20 mg —
Subject Lenalidomide Other / unclassified 25 mg —