An Open-Label, Dose Finding Study to Investigate the Safety, Pharmacokinetics, and Preliminary Efficacy of BMCA and GPRC5D dual target CAR-T cells therapy in Patients with relapsed or refractory multiple myeloma
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
9
Patients will receive lymphodepleting chemotherapy followed by a single infusion of OriC321
Incidence, severity AEs/SAEs
Time frame: 2 years after CAR-T cell infusion
Concentration of CAR-T cells
Time frame: 2 years after CAR-T cell infusion
Objective response rate (ORR)
Time frame: 2 years after CAR-T cell infusion
Progression-free survival (PFS)
Time frame: 2 years after CAR-T cell infusion
Duration of response (DOR)
Time frame: 2 years after CAR-T cell infusion
Overall survival (OS)
Time frame: 2 years after CAR-T cell infusion
Percentage of Patients With Negative Minimal Residual Disease (MRD)
Time frame: 2 years after CAR-T cell infusion
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