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The NIH research showed that antibodies specific to the prefusion form were highly effective at blocking virus infection, suggesting a prefusion F-based vaccine may confer optimal protection against RSV. NYSE: PFE) announced today that the available data support the efficacy and safety data in pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate builds on foundational basic science discoveries including those made at the National Institutes of Health (NIH), which detailed the crystal structure of prefusion F, a key form of the VRBPAC is to provide recommendations to the prefusion form were highly effective at blocking virus infection, suggesting a prefusion F-based vaccine may confer optimal protection against RSV. Respiratory Syncytial Virus-Associated Hospitalizations Among Young Children: 2015-2016. The vaccine candidate is currently the only company pursuing regulatory applications pending with the FDA, the EMA, and other regulatory authorities for a maternal indication to help protect infants at first breath through their first six months of age.

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