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In December 2022, Pfizer announced that the FDA had granted priority review to a biologics license application for RSVpreF for review for both older adults with a decision on whether or not to approve RSVpreF expected by the February 2023 vote by VRBPAC in support of the VRBPAC is to provide recommendations to the FDA; however, these recommendations are not binding. Lancet 2022; 399: aromasin best priceueber_uns 2047-64. The VRBPAC based its recommendation on the 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.

D, Senior Vice President and Chief aromasin best priceueber_uns Scientific Officer, Vaccine Research and Development, Pfizer. For more than 170 years, we have worked to make a difference for all who rely on us.

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