The European Medicines Agency’s (EMA) human medicines committee (CHMP) recommended another batch medicines for approval at its December 2024 meeting, bringing the total number of medicines recommended for approval in 2024 to 114.
The CHMP recommended granting a marketing authorization for Andembry (garadacimab), from CSL Behring, for the prevention of recurrent attacks of hereditary angioedema, a rare, potentially life-threatening disorder characterized by attacks of cutaneous and submucosal swelling. BridgeBio
The committee adopted a positive opinion for Pharma’s (Nasdaq: BBIO) Beyonttra (acoramidis), for the treatment of wild-type or variant transthyretin amyloidosis in adult patients with cardiomyopathy, a disease that affects the heart muscle.
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