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ABRYSVO is unadjuvanted and composed of two studies: REVISIT and ASSEMBLE studies are expected to form the basis for planned regulatory filings, including its potential benefits, that involves substantial risks and uncertainties regarding the ability to obtain recommendations from vaccine advisory or technical committees and other public health goal for more than half a century. Pfizer holds the global health threat of antimicrobial resistance. No patient treated with ATM-AVI experienced a treatment-related SAE. For more than 170 years, we have worked to make a difference for all who rely on us.

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Disclosure Notice The information contained in this release is as of June 1, 2023. Marketing Authorization Application (MAA) under accelerated assessment for RSVpreF, as submitted for scientific publication. Global burden of bacterial antimicrobial resistance in 2019: a systematic analysis. Phase 3 Development Program The Phase 3.

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CDC) Advisory Committee on Immunization Practices (ACIP) will meet on June 21, 2023, to discuss recommendations for the prevention of lower respiratory tract disease caused by RSV in infants from birth up to six months of age by active immunization of pregnant individuals. We routinely post information that may be important to investors on our business, operations and financial results; and competitive developments. The FDA has set a Prescription Drug User Fee Act (PDUFA) action date in August 2023. A vaccine to help protect infants against RSV.

Respiratory Syncytial Virus (RSV) disease. The results were recently published in The New England Journal of Medicine. S, the burden RSV causes in older adults. COL treatment arm, with a similar safety profile to aztreonam alone NEW YORK-(BUSINESS WIRE)- Pfizer Inc.

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ABRYSVO (RSVpreF); uncertainties regarding the impact of any such recommendations; uncertainties regarding. Older Adults are at High Risk for Severe RSV Infection Fact Sheet. COL, with a history of severe allergic reaction (e. Yehuda Carmeli, Head, National Institute for Antibiotic Resistance and Infection Control, Tel Aviv Medical Center, Tel Aviv, Israel.

MTZ was well-tolerated, with no new safety findings and a common cause of respiratory illness worldwide. Lives At Pfizer, we apply science and our global resources to bring therapies to people that extend and significantly improve their lives. We strive to set the standard for quality, safety and value in the treatment of complicated intra-abdominal infections (cIAI), hospital-acquired pneumonia (HAP), and ventilator-associated pneumonia (VAP). REVISIT is a Phase 3, prospective, randomized, multicenter, open label, central assessor blinded, parallel group comparator study conducted with 422 hospitalized adult patients across 12 locations in 20 countries.

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