Lilly said the drug, which is branded as Olumiant, in combination
remdesivir showed a roughly one-day reduction in median recovery
time versus patients treated with remdesivir alone.
Based on the results from the trial, which tested more than 1,000
patients, Lilly said it plans to discuss the potential for an
emergency use authorization (EUA) with the U.S. Food and Drug
Administration.
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Remdesivir is at the forefront of the fight against COVID-19 after the drug was
granted an EUA in May after trial data showed the antiviral drug helped shorten
hospital recovery time.
The drug, which has been licensed by Lilly from Incyte Corp, could potentially
help suppress a potentially lethal immune response to COVID-19 called "cytokine
storm".
(Reporting by Manas Mishra in Bengaluru; Editing by Saumyadeb Chakrabarty)
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