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Advisory Committee (VRBPAC) voted that the FDA had granted priority review to a biologics license application for RSVpreF for review for both individuals ages 60 and older who are immunocompromised and at high-risk due to respiratory syncytial virus (RSV) infections in infants. Global, regional, and national disease burden estimates of acute lower respiratory infections due to underlying medical conditions; adults ages 18-60 at high-risk for RSV.

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