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NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for review 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 age. NYSE: PFE) announced today that the available data support the efficacy and safety of its emulgel 50 gr medicationfaire_jecken?jahr=2010 unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. Earlier this month, Pfizer also announced it would be initiating multiple clinical trials evaluating RSVpreF in healthy children ages 5-18 with underlying medical conditions; adults ages 18 and older and as a maternal immunization vaccine to help protect infants against RSV. Lancet 2022; 399: 2047-64.
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