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GSK Reports the US FDA Approval of Penmenvy (MenABCWY Vaccine) for Protection Against Invasive Meningococcal Disease (IMD)
Shots:
- The US FDA has approved Penmenvy for individuals (10-25yrs) to protect against 5 serogroups of N. meningitidis (A, B, C, W, & Y) responsible for IMD. Meanwhile, the CDC's ACIP will vote on Feb 26, 2025, to recommend the use of Penmenvy in adolescents & young adults
- Approval was supported by 2 P-III trials (2019-001666-15 & 2019-004982-42) assessing the vaccine's safety, tolerability, & immune response in ~4800 subjects (10-25yrs.) that showed consistent safety
- Penmenvy integrates antigenic properties of lyophilized Menveo (MenACWY vaccine), which is reconstituted using a prefilled syringe of liquid Bexsero (MenB Vaccine)
Ref: GSK | Image: GSK
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Ridhi is an avid secondary researcher who follows trends in the biopharmaceutical and healthcare sectors to curate engaging content for the global audience. She works as a news editor at PharmaShots and loves to read books and explore new destinations.