FDA broadened existing EUA of Lilly and Incyte’s baricitinib in patients hospitalized with COVID-19

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On Jul. 29, 2021, Incyte announced the U.S. Food and Drug Administration (FDA) had broadened the Emergency Use Authorization (EUA) for baricitinib to allow for treatment with or without remdesivir, whereas the EUA was previously restricted to use only in combination with remdesivir.

The EUA now provided for the use of baricitinib for treatment of COVID-19 in hospitalized adults and pediatric patients two years of age or older requiring supplemental oxygen.

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Source: PR Nreswire
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