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Pfizer announces FDA approval for Abrysvo RSVpreF vaccine

Pfizer announced that the FDA has approved Abrysvo, the company’s bivalent RSV prefusion F, or RSVpreF, vaccine, for the prevention of LRTD and severe LRTD caused by RSV in infants from birth up to six months of age by active immunization of pregnant individuals at 32 through 36 weeks gestational age. Abrysvo is unadjuvanted and composed of two preF proteins selected to optimize protection against RSV A and B strains.

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