IASO Biotherapeutics’ Equecabtagene Autoleucel, the World’s First CAR-T for Treatment of NMOSD, Receives IND Application Acceptance by NMPA – QNT Press Release


SAN JOSE, Calif., NANJING, China and SHANGHAI, May 28, 2022 /PRNewswire/ — IASO Biotherapeutics (IASO Bio), a clinical-stage biopharmaceutical company engaged in discovering, developing, and manufacturing innovative cell therapies and antibody products, announced today that China’s National Medical Products Administration (NMPA) has accepted its investigational new drug (IND) application for the new extended indication of Neuromyelitis Optica Spectrum Disorder (NMOSD) for a fully human BCMA chimeric antigen receptor autologous T (CAR-T) cell Injection (Equecabtagene Autoleucel,CT103A). This NMPA acceptance, the world’s first IND application for CAR-T in NMOSD.

IASO Bio’s IND application is based on the Equecabtagene Autoleucel Investigator Initiated Trial (IIT) enrolling patients with refractory NMOSD who were positive for Aquaporin 4 antibodies (AQP4). Subjects enrolled were patients with poor symptom control despite at least one year of treatment with at least one immunosuppressant. The primary endpoint of this study was to observe the safety and tolerability, as well as preliminary efficacy, pharmacokinetic (PK), and pharmacodynamic (PD) related indicators in subjects with relapsed/refractory NMOSD treated with Equecabtagene Autoleucel. As of March 20, 2022 cut-off date, 12 subjects received Equecabtagene Autoleucel cell reinfusion, including three in the 0.5×106 CAR-T cells/kg dose group, three in the 1.0×106 CAR-T cells/kg dose group in the dose escalation stage and six subjects in the expansion stage.

The preliminary data presented safety and efficacy of Equecabtagene Autoleucel in the 0.5×106 CAR-T cells/kg and 1.0×106 CAR-T cells/kg dose groups in treatment of NMOSD patients suffering from conditions that were poorly controlled by conventional therapies. All of them experienced 1~2 CRS and no ICANS events prescribed in the protocol were found in the dose exploration period of 12 subjects . …

Full story available on Benzinga.com



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