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Talicabtagene autoleucel is a humanized anti-CD19 chimeric antigen receptor (CAR) T-cell therapy developed for the treatment of relapsed/refractory B-cell malignancies. It consists of autologous T cells from the patient that have been genetically modified to express a humanized anti-CD19 CAR. The therapy is administered as a single intravenous infusion and has demonstrated high response rates in clinical trials for patients with relapsed/refractory B-cell lymphomas and acute lymphoblastic leukemia. Talicabtagene autoleucel was first approved in India in October 2023 for these indications[3][5][2].
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