Merck to seek emergency authorization for oral Covid treatment after ‘compelling results’ in trials
- A phase 3 trial of Merck and Ridgeback Biotherapeutics’ oral antiviral treatment molnupiravir showed it reduced the risk of hospitalization or death by around 50% in Covid-19 patients.
- Merck plans to seek Emergency Use Authorization in the U.S. and submit marketing applications to other global drug regulators.
- If authorized by regulatory bodies, molnupiravir could be the first oral antiviral medicine for Covid-19.