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Rha B, Curns AT, Lively JY, et al. The bivalent vaccine candidate is composed of equal amounts of recombinant RSV prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for review for the prevention of RSV disease in older adults with a decision on whether or not to approve RSVpreF expected by thePDUFA goal date in August 2023. Scheltema NM, Gentile A, Lucion F, et al.

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Global, regional, and national disease burden estimates of acute lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in infants less than 12 months of age. If approved, our RSV vaccine candidate would help protect infants against RSV. RSVpreF), including its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc.

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