JUST IN: Vaccine advisers to the FDA have voted unanimously to recommend emergency use authorization of a booster dose of Moderna's Covid-19 vaccine for certain groups
The FDA's Vaccines and Related Biological Products Advisory Committee agreed use of a booster dose would be safe and effective in some people six months out from their primary series.Moderna had asked for emergency use authorization for a half dose of its vaccine to be used as a booster for certain people.
The FDA's committee of independent advisers typically discusses and makes recommendations to the agency around vaccine authorizations and approvals, and the agency then makes the final decision about whether to OK a vaccine. If the FDA gives emergency use authorization to Moderna boosters, vaccine advisers to the US Centers for Disease Control and Prevention will meet to discuss which groups to recommend them to.
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