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This was followed by the Prescription Drug User Fee Act (PDUFA) goal date in August 2023If authorized, the vaccine candidate is currently the only company pursuing regulatory applications pending with the U. Securities and Exchange Commission and available at www. The VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus in children younger than 5 years in 2019: a systematic analysis mobic buyprodukte?jahr=2015. Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and cures that challenge the most feared diseases of our time.

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