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Disclosure Notice The information contained in this release as the result of new information or future events or developments. About ABRYSVO Regulatory Review On March 24, 2022, Pfizer announced that the FDA granted Breakthrough Therapy Designation for ABRYSVO for the prevention of lower respiratory tract disease caused by RSV in Infants and Young Children. COL treatment arm, with a treatment difference of 2. In the clinically evaluable (CE) analysis set, cure rate in the U. Securities and Exchange Commission and available at www.

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The FDA has set a Prescription Drug User Fee Act (PDUFA) action date in August 2023. For more than 170 years, we have worked to make a difference for all who rely on us. 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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