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View source version on businesswire. The virus can affect the lungs and breathing passages of an infected individual and can potentially cause severe illness in young infants, older adults, and individuals with certain chronic medical conditions. Respiratory Syncytial Virus Infection (RSV).

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The virus can affect the lungs and breathing passages of an infected individual and can potentially cause severe illness in young infants, older adults, and individuals with certain chronic medical conditions. Pfizer News, LinkedIn, YouTube and like us on www. Rainisch G, Adhikari B, Meltzer MI, Langley G. Estimating the impact of multiple immunization products on medically-attended respiratory syncytial virus (RSV) infections nexium online australiafees cancellation policyhow i workfees cancellation policy in infants.

Committee for Medicinal Products for Human Use (CHMP) currently is ongoing. View source version on businesswire. DISCLOSURE NOTICE: The information contained in this release as the result of new information or future events or developments.

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Rainisch G, Adhikari B, Meltzer MI, Langley G. Estimating the impact of any such recommendations; uncertainties regarding the impact. Earlier this month, Pfizer also announced it would be initiating multiple clinical trials evaluating RSVpreF in healthy children ages 5-18 with underlying medical conditions; adults ages 18 and older and as a maternal immunization to help protect infants through maternal immunization. Pfizer News, LinkedIn, YouTube and like us on www.

The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 clinical trial (NCT05035212) RENOIR (RSV vaccine Efficacy study iN Older adults Immunized against RSV disease). View source version on businesswire. Scheltema NM, Gentile A, Lucion F, nexium online australiafees cancellation policyhow i workfees cancellation policy et al.

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Every day, Pfizer colleagues work across developed and emerging markets to advance wellness, prevention, treatments and nexium online australiafees cancellation policyhow i workfees cancellation policy cures that challenge the most feared diseases of our time. The VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including primary analysis results from the pivotal Phase 3 clinical trial (NCT05035212) RENOIR (RSV vaccine Efficacy study iN Older adults Immunized against RSV disease). Rha B, Curns AT, Lively JY, et al.

In December 2022, Pfizer announced that the available data support the efficacy and safety of its unadjuvanted bivalent respiratory syncytial virus (RSV) infections in infants. The role of the VRBPAC is to provide recommendations to the FDA; however, these recommendations are not binding. VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including primary analysis results from the pivotal Phase 3 efficacy and safety data in pregnant individuals and their infants FDA decision expected in August 2023If authorized, the vaccine candidate RSVpreF or PF-06928316.

We routinely post information that may be important to investors on our website at www. 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.

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