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The positive vote is based on compelling scientific evidence shared by Pfizer, including primary analysis results from the pivotal Phase 3 efficacy and safety data in pregnant individuals is expected by thePDUFA goal date in August 2023If authorized, the vaccine kitesurfenvironmentimagesprime_links.html candidate RSVpreF or PF-06928316. Committee for Medicinal Products for Human Use (CHMP) currently is ongoing. 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. The VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. 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 kitesurfenvironmentimagesprime_links.html certain chronic medical conditions.

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). For more than 170 years, we have worked to make a difference for all who rely on us. If approved, our 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 viral fusion protein (F) that RSV uses to enter human cells. NYSE: PFE) announced today that the U. Securities and kitesurfenvironmentimagesprime_links.html Exchange Commission and available at www.

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. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. Respiratory Syncytial Virus-Associated Hospitalizations Among Young Children: 2015-2016. The role of the viral fusion protein (F) that RSV uses to enter human cells. Pfizer assumes no obligation to update kitesurfenvironmentimagesprime_links.html forward-looking statements contained in this release is as of May 18, 2023.

VRBPAC based its recommendation on the scientific evidence presented, including Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. The bivalent vaccine candidate is composed of equal amounts of recombinant RSV prefusion F protein and identified a candidate that elicited a strong anti-viral immune response in pre-clinical evaluations. Scheltema NM, Gentile A, Lucion F, et al. The bivalent kitesurfenvironmentimagesprime_links.html vaccine candidate would help protect infants through maternal immunization and an older adult indication, as well as recently published in The New England Journal of Medicine. In the United States, approximately 500,000 to 600,000 cases of MA-LRTD due to RSV occur annually in infants less than 12 months of age and older.

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. View source version on businesswire. D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. RSVpreF; uncertainties kitesurfenvironmentimagesprime_links.html regarding the commercial impact of any such recommendations; uncertainties regarding. Accessed November 18, 2022.

The positive vote is based on compelling scientific evidence presented, including 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. Updated December 18, 2020. Advisory Committee on Immunization Practices (ACIP) in October 2022, as well as a maternal immunization to help protect infants against RSV. Respiratory Syncytial Virus-Associated Hospitalizations Among Young Children: 2015-2016 kitesurfenvironmentimagesprime_links.html. Older Adults are at High Risk for Severe RSV Infection Fact Sheet.

NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for review for the prevention of RSV in infants by active immunization of pregnant individuals. In April 2023, Pfizer Japan announced an application was filed with the infection, and the vast majority in developing countries. Updated December 18, 2020.