drugset / Trial / NCT01206205

Frontline Therapy in de Novo Multiple Myeloma Patients Under 65

NCT01206205 ↗

NaSingle-groupOpen-labelTreatment

Summary

The purpose of this Phase 2 study is to evaluate the efficacy and safety of treatment with bortezomib, lenalidomide and dexamethasone in patients with untreated multiple myeloma. This study will evaluate whether the addition of lenalidomide to bortezomib and dexamethasone will increase the Complete Response (CR)/ very good partial response (VGPR) rate before and after High Dose Therapy (HDT) with ASCT.

Timeline

Start
2009-08
Primary completion
2012-10
Completion
2012-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Bortezomib Small molecule 1.3 mg/m2 —
Subject Dexamethasone Small molecule 40 mg —
Subject Lenalidomide Other / unclassified 10 mg —

Indications