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In December 2022, Pfizer announced that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of RSV disease and its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc. DISCLOSURE NOTICE: The information contained in this release is as of May 18, 2023. If approved, our RSV vaccine candidate is composed of equal best price Capoten 25 mg amounts of recombinant RSV prefusion F vaccine candidate. The NIH research showed that antibodies specific to the prefusion form were highly effective at blocking virus infection, suggesting a prefusion F-based vaccine may confer optimal protection against RSV. In December 2022, Pfizer announced that the available data support the efficacy and safety data in pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate has the potential to be the first maternal immunization to help protect infants against RSV.
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