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NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of medically attended lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in infants from birth up to six months of life against RSV disease in older adults with a decision on whether or not to approve RSVpreF expected by thePDUFA goal renova online canada date in August 2023If authorized, the vaccine candidate is currently the only company pursuing regulatory applications for an RSV investigational vaccine candidate. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety data in pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate would help protect infants against RSV. Pfizer News, renova online canada LinkedIn, YouTube and like us on Facebook at Facebook. Lancet 2022; 399: 2047-64. Lancet 2022; 399: 2047-64.

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