Moderna Secures FDA Approval for RSV Vaccine mRESVIA for At-Risk Adults Aged 18-59

Reuters
13 Jun
Moderna Secures FDA Approval for RSV Vaccine mRESVIA for At-Risk Adults Aged 18-59

Moderna Inc. has announced that the U.S. Food and Drug Administration (FDA) has approved their RSV vaccine, mRESVIA® (mRNA-1345), for adults aged 18-59 who are at increased risk for respiratory syncytial virus (RSV) disease. This expands the vaccine's previous approval for adults aged 60 and older, granted in May 2024. The approval is based on results from Moderna's Phase 3 study, which showed the vaccine to be well-tolerated and effective in generating immune responses in the younger at-risk population. Moderna plans to have mRESVIA available for both younger and older adults in the U.S. for the 2025-2026 respiratory virus season.

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