FDA Approves Ensitrelvir to Prevent COVID-19 After Exposure
Conexiant
June 2, 2026
The FDA has approved ensitrelvir (XOCOVA) for postexposure prophylaxis of COVID-19 in individuals aged 12 and older.
Ensitrelvir is the first oral option approved to prevent COVID-19 following exposure to an infected individual.
The approval was based on the phase 3 SCORPIO-PEP trial, which enrolled 2,387 participants exposed to symptomatic COVID-19.
Ensitrelvir reduced the risk of symptomatic COVID-19 by 67% compared to placebo among uninfected participants.
The most common adverse events with ensitrelvir were headache, diarrhea, and cough, with overall rates similar to placebo.
This content is an AI-generated, fully rewritten summary based on a published scholarly article. It does not reproduce the original text and is not a substitute for the original publication. Readers are encouraged to consult the source for full context, data, and methodology.
Stay up to date with the latest clinical headlines and other information tailored to your specialty.
Thank you for signing up for the Daily News alerts. You will begin receiving them shortly.
Editor
Affiliations:
Specialties:
Areas of Expertise: