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If approved, our RSV vaccine candidate would help protect infants at first breath through six months of life from this potentially serious infection. The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety data in pregnant individuals is expected by the Prescription Drug User Fee Act (PDUFA) goal date later this month. We strive to set the standard for quality, safety and how do i get protopic effectiveness of RSVpreF in adults 60 years of age and older.

Updated December 18, 2020. After this important discovery, Pfizer tested numerous versions of a stabilized prefusion F from subgroups A and B. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus how do i get protopic (RSV) prefusion F vaccine candidate is currently under FDA review for the prevention of RSV disease and its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc.

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