drugset / Trial / NCT00044382

Study of the Safety and Efficacy of CC-5013 Treatment For Patients With Myelodysplastic Syndrome

NCT00044382 ↗

Phase 2 Completed 25 enrolled Celgene Corporation
RandomizedSingle-groupOpen-labelTreatment

Summary

To estimate the percent of patients with myelodysplastic syndromes (MDS) who experience erythroid response and the interval to response with daily treatment of 25 mg of CC-5013 .

Timeline

Start
2002-02-01
Primary completion
2007-01-01
Completion
2007-01-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 25 mg —