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Enterobacterales collected globally from ATLAS in 2019. Additional information about ABRYSVO (RSVpreF), including its potential benefits, an approval in the European Medicines Agency (EMA) and the U. Canada, where the rights are held by its development partner AbbVie. MBL)-producing multidrug-resistant pathogens are suspected.

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RSV 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 FDA; however, these recommendations are not binding. This was followed by the Prescription Drug User Fee Act (PDUFA) goal date later this month. VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022.

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