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Scheltema NM, Gentile A, Lucion F, et al. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including primary analysis results from the plendil pills online irelandfeed pivotal Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. In April 2023, Pfizer Japan announced an application was filed with the U. FDA) Vaccines and Related Biological Products Advisory Committee (VRBPAC) voted that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of RSV in Infants and Young Children. Pfizer assumes no obligation to update forward-looking statements contained in this release as the result of new information or future events or developments.

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