Eli Lilly and Company plans to seek an emergency use authorization from the US Food and Drug Administration and similar go-aheads in other countries for Olumiant (baricitinib) in the treatment of hospitalized COVID-19 patients based on results from a US National Institute of Allergy and Infectious Disease study of the JAK1/2 inhibitor in combination with Gilead Sciences, Inc.’s Veklury (remdesivir).
Olumiant, which showed a statistically significant improvement versus remdesivir alone in time to recovery, was developed under a partnership with...








