drugset / Trial / NCT01568294

Japanese Phase 1 Study to Evaluate Tolerated Dose, Safety, and Efficacy of Pomalidomide in Patients With Refractory or Relapsed and Refractory Multiple Myeloma

NCT01568294

Phase 1 Completed 12 enrolled Celgene Corporation
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine the tolerated dose of pomalidomide and also to evaluate the pharmacokinetics, safety and efficacy of pomalidomide in patients with refractory or relapsed and refractory multiple myeloma.

Timeline

Start
2012-04-01
Primary completion
2015-07-08
Completion
2015-07-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Pomalidomide Other / unclassified 2 mg Oral
Subject Pomalidomide Other / unclassified 4 mg Oral

Indications