BioCentury
ARTICLE | Clinical News

FDA grants Amgen's Blincyto accelerated approval for MRD-positive ALL

March 30, 2018 3:35 PM UTC

FDA granted accelerated approval to Blincyto blinatumomab to treat B cell precursor acute lymphoblastic leukemia in patients who are in remission but still have minimal residual disease (MRD). The bispecific T cell engager (BiTE) against CD19 is the first drug FDA has approved to treat the condition...

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Amgen Inc.

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CD19