Determining the Feasibility of MLN9708 as Maintenance After Allogeneic Stem Cell Transplant for Multiple Myeloma

PHASE2CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

September 30, 2014

Primary Completion Date

February 1, 2019

Study Completion Date

February 1, 2019

Conditions
Multiple Myeloma
Interventions
DRUG

MLN9708

"Patients will be enrolled between Days 45 and 120 after allogeneic transplant and will receive MLN9708 orally (PO) as monotherapy on Days 1, 8, and 15 of each 28-day cycle for 6 cycles. Up to 18 patients will be enrolled in a dose-escalation phase to determine the maximum tolerated dose (MTD).~Dose-Escalation Phase: MLN9708 will be administered orally (PO) as monotherapy. Dosing will start at 2.3 mg. If acceptable tolerability is demonstrated, escalations will be made to 3 mg and to a maximum-planned dose (MPD) of 4 mg."

Trial Locations (4)

37203

Tennessee Oncology PLLC, Nashville

45242

Oncology Hematology Care, Cincinnati

78229

Texas Transplant Institute, San Antonio

80218

Colorado Blood Cancer Institute, Denver

Sponsors
All Listed Sponsors
collaborator

Millennium Pharmaceuticals, Inc.

INDUSTRY

lead

SCRI Development Innovations, LLC

OTHER