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BeiGene announces FDA approval of Brukinsa for CLL
The Fly

BeiGene announces FDA approval of Brukinsa for CLL

BeiGene announced that the FDA has approved its Bruton’s tyrosine kinase inhibitor, BTKi, Brukinsa for the treatment of adult patients with chronic lymphocytic leukemia, CLL, or small lymphocytic lymphoma, SLL. The U.S. approval is based on two global Phase 3 clinical trials demonstrating superior efficacy and a favorable safety profile for Brukinsa in CLL.

Published first on TheFly

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