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cnet.comVRBPAC voted unanimously on June 18 that benefits outweigh risks for adults ages 50-64 and 65+. The final FDA decision on licensure remains pending.
abcnews.go.comAn advisory committee voted unanimously Thursday to support licensure of the shot for adults aged 50–64 via the traditional pathway and for adults 65 and older via the accelerated pathway. The FDA is expected to decide by August 5.
Substrate placeholder — needs reviewModerna has received marketing authorization from the European Commission for MCOMBRIAX, its mRNA combination vaccine against influenza and COVID-19. This enables distribution in European markets. The vaccine targets respiratory viruses with combined protection.