drugset / Trial / NCT00463385

A Phase II Study of Pomalidomide in Myelofibrosis With Myeloid Metaplasia

NCT00463385

Phase 2 Completed 88 enrolled Celgene Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The purpose of this study is to determine the safety of and to select a treatment regimen of pomalidomide (CC-4047) either as single-agent or in combination with prednisone to study further in patients with myelofibrosis with myeloid metaplasia (MMM).

Timeline

Start
2007-04-01
Primary completion
2009-05-01
Completion
2013-12-31

Publications

  • Background Barosi G, et al. Decrease Of T Regulatory Cells In Patients With Myelofibrosis Receiving Ruxolitinib. Presented at American Society of Hematology 2013, December 7-10, 2013, New Orleans, LA. Abstract No. 4057. Blood, 2013;122(21)

Drugs

EvaluationDrugModalityDoseRoute
Subject Pomalidomide Other / unclassified 0.5 mg Oral
Subject Pomalidomide Other / unclassified 2 mg Oral
Subject Prednisone Other / unclassified 15 mg Oral