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Lilly Gets Second EUA, For Baricitinib In COVID-19 Patients

 
• By Joseph Haas

Weeks after FDA authorized emergency use of its antibody bamlanivimab, Lilly’s RA drug Olumiant can be used to shorten recovery time for hospitalized COVID-19 patients in the US. Authorizations are being pursued elsewhere as well.

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Lilly's second EUA for a COVID-19 therapy covers Olumiant in hospitalized patients

Eli Lilly and Company got a second emergency use authorization for a COVID-19 therapy on 19 November, this time for its rheumatoid arthritis drug Olumiant (baricitinib) as part of combination therapy with Gilead Sciences, Inc.’s Veklury (remdesivir) in hospitalized patients who require supplemental oxygen. Previously, its experimental neutralizing antibody bamlanivimab got EUA approval from the US Food and Drug Administration earlier this month to treat patients with mild-to-moderate COVID-19 symptoms.

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