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Pfizer reports EC approval of amending marketing authorization of Abrysvo

Pfizer (PFE) announced that the European Commission has issued a decision amending the marketing authorization for Abrysvo, the company’s bivalent respiratory syncytial virus prefusion F vaccine, to extend the indication to include prevention of lower respiratory tract disease caused by RSV in individuals 18 through 59 years of age, expanding the previous authorization for individuals aged 60 and older.

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