Key Takeaways
- The FDA cancelled the 13 March VRBPAC meeting intended to select strains for the 2025-2026 flu vaccine for the Northern Hemisphere.
- Because companies need about six months to manufacture the vaccine in time for the start of flu season, the delay could impact availability.
- The VRBPAC meeting cancellation follows the CDC postponing the 26-28 February Advisory Committee on Immunization Practices meeting.
The US Food and Drug Administration has cancelled the 13 March meeting of its Vaccines and Related Biological Products Advisory Committee, which was
Committee member Paul Offit, a pediatrics professor in the Division of Infectious Diseases at the Children’s Hospital of Philadelphia, confirmed to the Pink Sheet that the agency emailed 26 February to notify him the meeting had been cancelled
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