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BeiGene's CD3/CD19 Dual Antibody Belintoumumab New Indication Approved

 Last Update: 2022-05-14
 Source: Internet
 Author: User

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On April 29, BeiGene's new indication of belintoumumab for injection submitted by BeiGene was approved by the State Food and Drug Administration for the treatment of relapsed or refractory precursor B-cell acute lymphoblastic leukemia in adults and children

Belintuumab is a CD3-CD19-targeting bispecific antibody developed based on Amgen's state-of-the-art Bispecific T Cell Engagement System (BiTE®)

Belintuumab was approved by the NMPA on December 4 last year through priority review for the treatment of adults with relapsed or refractory precursor B-cell acute lymphoblastic leukemia (ALL)

Belintoumumab was first approved by the FDA in December 2014

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