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Vertex announces U.S. FDA approval for label extensions of Alyftrek, Trikafta

Vertex Pharmaceuticals (VRTX) announced the U.S. Food and Drug Administration, FDA, has approved expanded use of Alyftrek for the treatment of people with cystic fibrosis ages 6 and older with a variant in the cystic fibrosis transmembrane conductance regulator, CFTR, gene that is either responsive based on clinical and/or in vitro data or results in production of CFTR protein. Additionally, the U.S. FDA has also expanded the indication statement for Trikafta in patients ages 2 and older.

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