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QI-019A is an innovative *in vivo* chimeric antigen receptor (CAR) T-cell gene therapy being developed for the treatment of relapsed or refractory multiple myeloma. Unlike traditional *ex vivo* CAR-T therapies that require leukapheresis and external cell manufacturing, QI-019A utilizes a lentiviral vector delivery system administered directly to the patient. This vector is designed to transduce and integrate into the genome of endogenous T cells, leading to the stable expression of a dual-targeting CAR transgene directed against B-cell maturation antigen (BCMA) and CD19. By generating CAR-T cells within the patient's body, QI-019A aims to simplify the treatment process and provide a potent anti-tumor response against malignant plasma cells.
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