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).
Lilly’s Olumiant Cuts COVID-19 Hospital Stays By One Day
Company Will Seek An EUA For Baricitinib Plus Remdesivir
Olumiant (baricitinib) plus Gilead’s Veklury (remdesivir) provided a statistically significant reduction in time to recovery versus remdesivir alone for hospitalized patients in US NIAID’s ACTT-2 clinical trial.
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