This is a multi-center, phase I trial that studies the efficacy and recommended dose of BCMA CART cells in treating patients with BCMA-positive multiple myeloma (MM) that have not respond or relapsed after chemotherapy. B-cell maturation antigen (BCMA), a cell surface protein expressed on malignant plasma cell, has emerged as a very selective antigen to be targeted in novel immunotherapy for MM.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
10
Each patient will receive BCMA Targeted CAR T-cells by intravenous infusion.
Incidence of adverse events (AEs)
Incidence of adverse events (AEs)
Time frame: Up to approximately 6 months
Dose limiting toxicities (DLTs)
Dose limiting toxicities (DLTs)
Time frame: Up to 21 days
Overall response rate (ORR)
Overall response rate (ORR)
Time frame: Up to approximately 6 months
Percentage of subjects who achieved complete response or strict complete response (CR/sCR)
Percentage of subjects who achieved complete response or strict complete response (CR/sCR)
Time frame: Up to approximately 6 months
Percentage of subjects who achieved very good partial response (VGPR) and higher response rate
Percentage of subjects who achieved very good partial response (VGPR) and higher response rate
Time frame: Up to approximately 6 months
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