The US regulator is expected to grant an Emergency Use Authorization (EUA) for the use of a booster shot of the coronavirus vaccine developed by Moderna (Nasdaq: MRNA).
The submission from the messenger RNA (mRNA) specialist included data from a Phase II study of mRNA-1273, in which people were given a half-dose six to eight months after their second regular dose.
The US Food and Drug Administration’s scientific panel voted unanimously in favor of granting the EUA for people over the age of 65 or at risk of severe complications from the disease.
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