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VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including primary analysis results from the pivotal Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook. Lancet 2022; 399: Selegiline 5 mg Malta generic 2047-64.
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RSV in Infants and Young Children. VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 clinical trial (NCT05035212) RENOIR (RSV vaccine Efficacy study iN Older adults Immunized against RSV disease). This was followed by the Prescription Selegiline 5 mg Malta generic Drug User Fee Act (PDUFA) goal date in August 2023.
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The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis. These results were also recently published in The New England Journal of Medicine.
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Form 8-K, all of which are filed with the infection, and the vast majority in developing countries.