FDA panel considers a first-of-its-kind flu vaccine using mRNA technology (opens original article in a new tab)
U.S. health advisers are evaluating Moderna's mRNA flu vaccine, which showed 27% effectiveness in reducing cases among adults 50 and older, with FDA noting no safety issues but incomplete data on vulnerable groups.
- FDA advisory committee is reviewing Moderna's mRNA flu vaccine for approval
- mFlusiva showed 27% reduction in flu cases among 50+ adults in a 40,000-person study
- FDA noted no safety concerns but lacks data on frail older adults and immunocompromised individuals
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