drugset / Trial / NCT01062152

Dose-Ranging Study of Telintra® Tablets + Revlimid® in Patients With Non-Deletion (5q) Low to Intermediate-1 Risk Myelodysplastic Syndrome (MDS)

NCT01062152 ↗

Phase 1 Completed 19 enrolled Telik
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This is an open label, multicenter Phase 1 dose escalation study evaluating five doses of ezatiostat in combination with lenalidomide in patients with non-del(5q) low to intermediate 1 risk MDS. The HI-E, HI-N, HI-P rates \[by International Working Group (IWG) 2006 criteria\] and safety of each treatment group will be evaluated to select the optimal dose of ezatiostat in combination with lenalidomide for future studies.

Timeline

Start
2009-11
Primary completion
2012-11
Completion
2013-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 10 mg Oral
Subject ezatiostat Small molecule 2000 mg Oral
Subject ezatiostat Small molecule 2500 mg Oral