Bendamustine, Wkly Bortezomib, Lenalidomide and Dexamethasone for Multiple Myeloma

PHASE1/PHASE2TerminatedINTERVENTIONAL
Enrollment

3

Participants

Timeline

Start Date

May 5, 2011

Primary Completion Date

June 18, 2014

Study Completion Date

June 18, 2014

Conditions
Multiple Myeloma
Interventions
DRUG

Bendamustine

The first group of three patients to enter the study will receive a 25 mg/m\^2 dose of bendamustine. If this dose is found to be safe, the next three patients will receive 50 mg/m\^2. Using a modified Fibonacci dose-escalation design, the dose will continue to increase at a rate of 25 mg/m\^2 until the highest safe dose of bendamustine is found. The maximum dose will be 125 mg/m\^2. Bendamustine and bortezomib will be given through a catheter twice a week every 21 days. Dexamethasone and lenalidomide will be given orally. In general, a cycle of chemotherapy will last 21 days.

Trial Locations (1)

60153

Loyola University Medical Center, Maywood

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Celgene

INDUSTRY

lead

Loyola University

OTHER

NCT01484626 - Bendamustine, Wkly Bortezomib, Lenalidomide and Dexamethasone for Multiple Myeloma | Biotech Hunter | Biotech Hunter