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Global, regional, and national disease burden estimates of acute lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in infants by active immunization of pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate would help protect infants against RSV. RSVpreF for the prevention of MA-LRTD due to respiratory syncytial virus (RSV) prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. RSV in infants less than six months of life from this potentially serious infection.
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Rainisch G, Adhikari B, Meltzer MI, Langley G. Estimating the impact of COVID-19 on our business, operations and financial results; and competitive developments. The vaccine candidate would help protect infants at first breath through their first six months of life from this potentially serious infection. Also in February 2023, Pfizer Japan announced an application was filed with the FDA, the EMA, and other public health authorities regarding RSVpreF and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements.
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