drugset / Trial / NCT01206205
Frontline Therapy in de Novo Multiple Myeloma Patients Under 65
Phase 2
Completed
31 enrolled
University Hospital, Toulouse
Celgene Corporation · collabJanssen-Cilag Ltd. · collab
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Bortezomib | Small molecule | 1.3 mg/m2 | — |
| Subject | Dexamethasone | Small molecule | 40 mg | — |
| Subject | Lenalidomide | Other / unclassified | 10 mg | — |