What Eli Lilly and Company calls proof-of-concept data for LY-CoV555, its neutralizing antibody candidate for the novel coronavirus, is meeting pushback from analysts, but a top Lilly exec told Scrip that the particulars and limitations of the dataset are less important than the demonstration that an antibody therapy can provide benefit to COVID-19 patients.
The Indianapolis pharma reported on 16 September that an interim analysis of the Phase II BLAZE-1 study showed that one of three investigational doses meets statistical significance on the primary endpoint of clearing the virus from baseline levels at day 11 after treatment and that pooled data for all three doses indicated a 72% reduction in risk of hospitalization for COVID-19 patients. In same-day notes, analysts wondered why the largest of three doses (700mg, 2
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?