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The positive vote is based on compelling scientific evidence shared by Pfizer, including primary analysis results from the pivotal Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for review for the prevention of MA-LRTD and severe MA-LRTD caused by RSV in Infants RSV is a contagious virus and a common cause of respiratory illness.
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