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The European Commission (EC) has granted conditional marketing approval for Bristol Myers Squibb & Co’s (NYSE: BMY) Abecma (idecabtagene vicleucel, ide-cel) for relapsed and refractory multiple myeloma. Abecma is a first-in-class B-cell maturation antigen (BCMA)-directed chimeric antigen receptor (CAR) T cell immunotherapy.
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