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TriPRIL CAR is an investigational chimeric antigen receptor T cell (CAR-T) therapy that uses a rationally designed trimeric APRIL-based binding domain to direct patient-derived T cells against multiple myeloma cells. The CAR targets both B-cell maturation antigen (BCMA) and transmembrane activator and CAML interactor (TACI), two TNFR superfamily members highly expressed on myeloma cells. This dual-targeted approach aims to overcome resistance stemming from single-antigen loss (antigen escape) and to expand efficacy for relapsed or refractory multiple myeloma. TriPRIL’s fully human construct also reduces immunogenicity and potential for antimurine immune rejection. TriPRIL CAR T Cells are produced via a rapid manufacturing process and are currently in early clinical testing, with Massachusetts General Hospital and King's College London noted as key development sites[1][2][3][4][5][6].
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