drugset / Trial / NCT00689936

Study to Determine Efficacy and Safety of Lenalidomide Plus Low-dose Dexamethasone Versus Melphalan, Prednisone, Thalidomide in Patients With Previously Untreated Multiple Myeloma

NCT00689936

Phase 3 Completed 1623 enrolled Celgene Corporation
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to compare the safety and efficacy of Lenalidomide plus low dose dexamethasone to that of the combination of melphalan, prednisone and thalidomide.

Timeline

Start
2008-08-21
Primary completion
2016-07-14
Completion
2016-07-14

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexamethasone Small molecule 20 mg Oral
Subject Dexamethasone Small molecule 40 mg Oral
Subject Lenalidomide Other / unclassified 2.5 mg Oral
Subject Lenalidomide Other / unclassified 5 mg Oral
Subject Lenalidomide Other / unclassified 10 mg Oral
Subject Lenalidomide Other / unclassified 15 mg Oral
Subject Lenalidomide Other / unclassified 20 mg Oral
Subject Lenalidomide Other / unclassified 25 mg Oral
Comparator Melphalan Small molecule 0.1 mg/kg Oral
Comparator Melphalan Small molecule 0.125 mg/kg Oral
Comparator Melphalan Small molecule 0.2 mg/kg Oral
Comparator Melphalan Small molecule 0.25 mg/kg Oral
Comparator Prednisone Other / unclassified 2 mg/kg Oral
Comparator Thalidomide Other / unclassified 100 mg Oral
Comparator Thalidomide Other / unclassified 200 mg Oral

Indications