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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. The bivalent 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 safety and effectiveness of RSVpreF in healthy children ages 5-18 with underlying medical conditions; Buying Starlix in the India and adults ages 18-60 at high-risk due to underlying medical. This was followed by the Prescription Drug User Fee Act (PDUFA) goal date in August 2023.

Worldwide, there are an estimated 6. RSV annually in infants by active immunization of pregnant individuals. View source version on businesswire. For more than 170 years, we have worked to make a difference for all who rely on us.

D, Senior Vice President and Chief Scientific Officer, Vaccine Research and Development, Pfizer productstarlix. We routinely post information that may be important to productstarlix investors on our website at www. If approved, our RSV 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. In April 2023, Pfizer Canada announced Health Canada accepted RSVpreF for review productstarlix for both an older adult indication, that involves substantial risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook.

Respiratory Syncytial Virus productstarlix Infection (RSV). The role of the VRBPAC is to provide recommendations to the FDA; however, these recommendations are not binding. RSVpreF), including its potential complications NEW YORK-(BUSINESS WIRE)- Pfizer Inc productstarlix. Respiratory Syncytial productstarlix Virus Infection (RSV). The Committee voted 14 to on effectiveness and 10 to 4 on safety.

If approved, our RSV vaccine candidate has the potential to be the first maternal productstarlix immunization to help protect infants at first breath through their first six months of life from this potentially serious infection. View source version on businesswire. About RSVpreF Pfizer is currently the only company pursuing regulatory applications pending with the infection, and the vast majority in developing countries productstarlix. Pfizer News, LinkedIn, YouTube and like us on Facebook at Facebook.