This trial aims to evaluate the safety and efficacy of BCMA-UCART in treating patients with r/r multiple myeloma.
This study is a non-randomized, open-label, single-arm clinical trial designed to assess the efficacy and safety of combination therapy for r/r multiple myeloma using universal CAR-T cells targeting BCMA .
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
6
The study drug is administered intravenously at a fixed dose within 1-2 days after lymphocyte depletion, and its efficacy and safety are observed.
Shanghi Tongji Hospital (Tongji Hospital of Tongji University)
Shanghai, China
RECRUITINGDLT
The number and severity of dose-limiting toxicity (DLT) events
Time frame: Within 28 Days After BRL-305 Infusion
AEs
The total number, incidence, and severity of AEs
Time frame: Up to 24 Months After BRL-305 Infusion
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