drugset / Trial / NCT01246076
Lenalidomide for Myelodysplastic Syndrome Refractory to Hypomethylating Agents
NaSingle-groupOpen-labelTreatment
Summary
The purpose of this study is to determine the proportion of confirmed responses (complete response, partial response, and hematologic improvement as defined by revised IWG criteria during the 12 months of treatment.
Timeline
- Start
- 2011-06
- Primary completion
- 2014-05
- Completion
- 2015-08
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Lenalidomide | Other / unclassified | 10 mg | — |