BCMA Targeted CAR T Cells With or Without Lenalidomide for the Treatment of Multiple Myeloma

PHASE1Active, not recruitingINTERVENTIONAL
Enrollment

20

Participants

Timeline

Start Date

February 27, 2017

Primary Completion Date

February 28, 2026

Study Completion Date

February 28, 2026

Conditions
Multiple Myeloma
Interventions
BIOLOGICAL

EGFRt/BCMA-41BBz CAR T cell

Modified T cell infusions will be administered 2-7 days following the completion of conditioning chemotherapy.There are 3 planned dose levels for this study: 1x10\^6, 3x10\^6, and 1x10\^7 EGFRt/BCMA-41BBz CAR T cells/kg, and a dose -1 level at 3x10\^5 EGFRt/BCMA-41BBz CAR T cells/kg, if needed; each dose cohort will consist of 3-6 patients.

DRUG

Cyclophosphamide

Cyclophosphamide 3000 mg/m2 IV once on day -7 to -2 or low intensity cy/flu (cyclophosphamide 300 mg/m2/day x 3 + fludarabine 30 mg/m2/day x 3) with the last day occurring on day -7 to -2 are the default options for is the default conditioning chemotherapy.

DRUG

Lenalidomide.

A cohort of patients will be treated with CAR T cell therapy and concomitant Lenalidomide. 10mg PO 21/28 days will be started no less then 1 week prior to clinical apheresis.

Trial Locations (1)

10065

Memorial Sloan Kettering Cancer Center, New York

All Listed Sponsors
collaborator

Juno Therapeutics, Inc., a Bristol-Myers Squibb Company

INDUSTRY

lead

Memorial Sloan Kettering Cancer Center

OTHER