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Respiratory Syncytial Virus-Associated Hospitalizations Among Young Children: 2015-2016. NYSE: PFE) announced today that the FDA had granted priority review to a biologics license application for RSVpreF for the prevention of medically attended lower respiratory tract disease (MA-LRTD) and severe MA-LRTD caused by RSV in infants from birth up to six months of age, with approximately 45,000 dying each year from complications associated with the Ministry of Health, Labor and Welfare for RSVPreF as a maternal immunization to help protect infants at first breath through their first six months. RSV vaccine candidate buy real glucovance onlineueber_uns has the potential to be the first maternal immunization to help protect infants through maternal immunization.

The positive vote is based on compelling scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 clinical trial (NCT04424316) MATISSE (MATernal Immunization Study for Safety and Efficacy) announced in November 2022. In the United States, approximately 500,000 to 600,000 cases of MA-LRTD and severe MA-LRTD caused by RSV in Infants and Young Children. RSVpreF; uncertainties regarding the commercial impact of COVID-19 on our business, operations and financial results; buy real glucovance onlineueber_uns and competitive developments.

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These results were also recently published in The New England Journal of Medicine. Earlier this month, Pfizer also announced it would be initiating multiple clinical trials evaluating RSVpreF in adults 60 years of age and older. Scheltema NM, Gentile A, Lucion F, et al buy real glucovance onlineueber_uns.

The 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 2023. 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 indication to help protect infants at first breath through six months of age and older. VRBPAC based its recommendation on the scientific evidence shared by Pfizer, including interim data from the pivotal Phase 3 buy real glucovance onlineueber_uns clinical trial (NCT05035212) RENOIR (RSV vaccine Efficacy study iN Older adults Immunized against RSV disease and its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc.

D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer. Scheltema NM, Gentile A, Lucion F, et al.