The company announced data on the combination of two antibodies against the SARS-CoV-2 virus, showing significant reductions in viral load compared with placebo. The company has applied for an EUA for LY-CoV555 and will seek an authorization for the combination of that drug with LY-CoV016 next month.
The company said that patients receiving LY-CoV555 at the 2,800mg dose showed a lower rate of hospitalization and emergency room visits than those on placebo. However, the other dose levels of the drug did not reach the viral load primary endpoint. An analyst called the data "mixed but constructive."
At the Abarca Forward conference earlier this year, George Van Antwerp, managing director at Deloitte, discussed how social determinants of health and a personalized member experience can improve medication adherence and health outcomes.