On Friday, the Food and Drug Administration Advisory Committee will review safety and efficacy data to see if they should expand Johnson & Johnson's emergency use authorization to include a booster shot for its COVID-19 vaccine. https://www.abcactionnews.com/news/coronavirus/fda-to-vote-on-j-j-covid-19-booster-shoots-also-looking-into-mixing-and-matching-vaccine-doses
The FDA Advisory Committee is meeting on Thursday to consider Moderna’s request for emergency use authorization for its booster shot. https://www.abcactionnews.com/news/coronavirus/fda-to-consider-moderna-covid-19-booster-shots-at-thursdays-advisory-committee-meeting
Merck is seeking FDA emergency use authorization for its experimental antiviral Covid-19 treatment, molnupiravir. If authorized, the drug would be the first oral antiviral treatment to fight Covid-19. CNN’s Elizabeth Cohen reports.