FDA Approves GSK’s 5-in-1 MenABCWY Vaccine
February 17, 2025
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2 min
The U.S. FDA approved the meningococcal groups A, B, C, W, and Y vaccine (Penmenvy) for patients aged 10 to 25 years. This pentavalent vaccine targets the major serogroups of Neisseria meningitidis responsible for invasive meningococcal disease (IMD). Data from phase III trials supported the approval and demonstrated a safety profile consistent with existing GSK meningococcal vaccines. The vaccine combines components from other vaccines, reducing the number of required injections. The approval aims to improve vaccination coverage, especially for IMD caused by serogroup B. The U.S. CDC's Advisory Committee on Immunization Practices is scheduled to vote on recommendations for the vaccine's use in adolescents and young adults in February 2025.
1. FDA approved Penmenvy vaccine for ages 10-25. 2. Targets major serogroups of Neisseria meningitidis. 3. Supported by phase III trial data. 4. Aims to improve vaccination coverage, especially for IMD caused by serogroup B. 5. U.S. CDC to vote on recommendations in February 2025.
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