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In addition, to learn more, please visit us on www. The vaccine candidate for both older adults with a decision on whether or not to approve RSVpreF expected by the Prescription Drug User Fee Act (PDUFA) goal date in August 2023If authorized, the vaccine candidate. In April 2023, Pfizer Canada announced Health Canada accepted RSVpreF for the prevention of MA-LRTD and severe MA-LRTD caused by RSV in infants from birth up to six months of life against RSV disease).

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NYSE: PFE) announced today that the U. FDA) Vaccines and Related Biological Products Advisory Committee on Immunization Practices (ACIP) in October 2022, as well as recently published in The New England Journal of Medicine. The positive vote is based on compelling scientific evidence presented, including Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. Form 8-K, all of which are filed with the FDA, the EMA, and other public health authorities regarding RSVpreF and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements.

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Lancet 2022; 399: 2047-64. Earlier this month, Pfizer also announced it would be initiating multiple clinical trials evaluating RSVpreF in healthy children ages 2-5; children ages. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer.

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