The disappointing benefit seen in Pfizer Inc.’s clinical study of Paxlovid (nirmatrelvir and ritonavir) in standard-risk COVID-19 patients suggests that even if the drug was authorized or approved for patients at standard risk as well as those at high risk of hospitalization and death, the oral antiviral is unlikely to get much uptake in the lower-risk population.
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?