In the USA, Cambridge-based Moderna (Nasdaq: MRNA) has requested an emergency use authorization (EUA) for its COVID-19 vaccine in adolescents.
The regulatory step follows positive Phase II/III data from the TeenCOVE study, announced in May.
The trial met its primary immunogenicity endpoint, successfully bridging immune responses to the adult vaccination, with no cases of COVID-19 observed in participants who had received two doses of the jab.
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