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FDA Advisory Committee votes in favor of Bristol Myers Squibb’s and 2seventy bio’s Abecma for triple-class exposed multiple myeloma in earlier lines of therapy

FDA to review Bristol Myers Squibb and 2seventy bio's Abecma, a CAR T cell therapy for relapsed or refractory multiple myeloma; the Oncologic Drugs Advisory Committee will assess data from the Phase 3 KarMMa-3 study in a virtual meeting

Regeneron announces formation of Regeneron Cell Medicines with the acquisition of 2seventy bio's full development and commercialization rights for novel immune cell therapies, along with discovery and clinical manufacturing capabilities

Bristol Myers Squibb and 2seventy bio report Abecma shows a 51% reduction in disease progression or death risk for multiple myeloma patients according to data from the KarMMa-3 study; it exhibited a safety profile consistent with previous studies

Bristol Myers Squibb and 2seventy bio provide update on FDA review of sBLA for Abecma idecabtagene vicleucel in earlier lines of therapy for triple-class exposed relapsed or refractory multiple myeloma

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