Gilead Sciences, Inc. is trying to clear up lingering questions about its COVID-19 therapeutic remdesivir with a new retrospective comparative analysis of its SIMPLE-Severe study, including showing a mortality benefit, which had not been evident in data used for global clearances for emergency use of the antiviral. But the select use of data without a controlled trial is drawing criticism.
The Foster City, CA-based company got a small stock bounce on 10 July after releasing retrospective comparative analysis data measuring remdesivir versus standard of care in patients hospitalized for COVID-19, but analysts and critics maintained that a traditional prospective trial is needed to confirm the company’s assertions of better clinical recovery and mortality outcomes with remdesivir
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?