Vertex Pharmaceuticals (Nasdaq: VRTX) has secured US Food and Drug Administration approval for a broader label for cystic fibrosis (CF) med Trikafta (elexacaftor/tezacaftor/ivacaftor and ivacaftor).
The approval covers certain children with CF aged six to 11, as defined by a particular genetic test, building on a previous nod in people aged 12 and over.
An additional dosage strength of Trikafta tablets is now available (elexacaftor 50mg/tezacaftor 25mg/ivacaftor 37.5mg and ivacaftor 75mg) in connection with the approval.
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