A senior Pfizer Inc. executive outlined, at a recent summit, some of the defining aspects of COVID-19 treatment Paxlovid’s (nirmatrelvir and ritonavir) development journey from first synthesis to first emergency use authorization (EUA). It was strikingly fast – speed with urgency and without cutting any corners for safety, as the executive put it.
Addressing the Organization of Pharmaceutical Producers of India (OPPI) summit, Pfizer’s senior vice president and chief scientific officer, bacterial vaccines and hospital, Dr Annaliesa Anderson, indicated that the oral antiviral had a four-month discovery phase, where the US company utilized its experience in “digital
Read the full article – start your free trial today!
Join thousands of industry professionals who rely on Scrip for daily insights
- Start your 7-day free trial
- Explore trusted news, analysis, and insights
- Access comprehensive global coverage
- Enjoy instant access – no credit card required
Already a subscriber?