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CBG002 is an autologous, armored BCMA-targeted CAR-T cell therapy engineered to constitutively express CD27, a costimulatory receptor. The addition of CD27 enhances T-cell proliferation and differentiation by binding its ligand CD70, resulting in improved persistence and cytotoxicity of the CAR-T cells. Preclinical studies demonstrated that CBG002 exhibits enhanced proliferation, greater cytotoxicity, and a higher proportion of memory T cells compared to conventional BCMA-CAR T cells. In animal models, it led to improved tumor control and prolonged survival in multiple myeloma xenograft mice. Clinically, phase I trials have shown that CBG002 is safe and effective for patients with relapsed or refractory multiple myeloma (RRMM), with an overall response rate of 81.8% and manageable adverse events[1][2][5].
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