Shionogi's ensitrelvir shows promise in COVID-19 prevention
Shionogi & Co., Ltd. (TSE:4507) announced positive results from its Phase 3 SCORPIO-PEP trial, revealing that ensitrelvir significantly reduces the risk of developing COVID-19 after exposure. The study demonstrated a 67% relative risk reduction in symptomatic COVID-19 among uninfected individuals treated with ensitrelvir compared to placebo at day 10 (risk ratio: 0.33; 95% CI: 0.22-0.49; p<0.0001). The primary analysis, involving 2,041 household contacts, showed that 2.9% of those treated with ensitrelvir developed symptomatic COVID-19 versus 9.0% in the placebo group. Ensitrelvir has received Fast Track designation from the U.S. FDA for post-exposure prophylaxis of COVID-19. Shionogi plans to continue engaging with regulatory authorities worldwide to bring this novel preventative treatment to market.
This report was generated by FilingReader's AI system from regulatory filings and company disclosures. To request a correction, contact editorial@filingreader.com
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