drugset / Trial / NCT00424047

A Study of CC-5013 Plus Dexamethasone Versus Dexamethasone Alone in Previously Treated Subjects With Multiple Myeloma

NCT00424047 ↗

Phase 3 Completed 351 enrolled Celgene Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

To compare the efficacy of oral CC-5013 in combination with oral pulse high-dose dexamethasone to that of placebo and oral high-dose pulse dexamethasone as treatment for subjects with relapsed or refractory multiple myeloma."

Timeline

Start
2003-01-01
Primary completion
2005-11-01
Completion
2013-11-12

Outcome

Met primary endpoint

registry Lenalidomide Plus Dexamethasone vs Placebo Plus Dexamethasone; p <0.001; Hazard Ratio (HR) 0.324 (95% CI 0.240 to 0.438); Log Rank NCT00424047 ↗

paper The time to progression was significantly longer in the patients who received lenalidomide plus dexamethasone PMID 18032762 ↗

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Lenalidomide Other / unclassified 25 mg Oral
Background Dexamethasone Small molecule 40 mg Oral

Indications