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US CDC’s Adult RSV Vaccine Recommendations In Flux With Impending FDA Approvals

 
• By Bridget Silverman

Moderna touts enriched Phase II/III population and severe RSV data as CDC advisory committee re-evaluates shared clinical decision-making and prepares for expected June votes on Moderna’s mRNA-1345 and expanded adult use of GSK’s Arexvy.

older woman coughing with cartoon of her lungs drawn over her image.
CDC will likely update its recommendations on adult RSV vaccines in June. • Source: Shutterstock

The US Centers for Disease Control and Prevention’s Advisory Committee on Immunization Practices laid the groundwork recently for what could be a momentous 26-28 June meeting for adult respiratory syncytial virus (RSV) vaccine policy.

Key Takeaways

  • CDC Advisory Committee on Immunization Practices is evaluating the experience of the first RSV season with approved vaccines as it re-evaluates its shared clinical decision-making recommendation for GSK’s Arexvy and Pfizer’s Abrysvo in adults ages 60 and older.

  • ACIP expects its June meeting will see votes on a third vaccine for adults ≥60 years, Moderna’s mRNA-1345, and a new use for GSK’s Arexvy in adults ages 50-59 at increased risk

The ACIP is revisiting the shared clinical decision-making status of its adult RSV recommendations while preparing for the impending approval of a third vaccine for adults ≥60

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