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Eli Lilly arthritis drug baricitinib in combination with remdesivir gets USFDA okay to treat Covid
New Delhi: The U.S. Food and Drug Administration on Thursday approved the emergency use of Eli Lilly and Co's arthritis drug, baricitinib, in combination with Gilead Sciences Inc's remdesivir, to treat COVID-19 patients.
Baricitinib, sold under the brand name of Olumiant, is an FDA-approved oral medication to treat moderately-to-severely active rheumatoid arthritis.
The approval was based on a review of the data from a clinical trial of hospitalized COVID-19 patients sponsored by the National Institute of Allergy and Infectious Diseases.
The trial showed an approximately one-day reduction in median recovery time for patients treated with the combination versus those treated with remdesivir.
Read also: Eli Lilly to acquire Disarm Therapeutics for USD 135 million
The health regulator approved the drug in combination with remdesivir for treating suspected or laboratory confirmed COVID-19 in hospitalized adults and children two years of age or older requiring oxygen support.
Ruchika Sharma joined Medical Dialogue as an Correspondent for the Business Section in 2019. She covers all the updates in the Pharmaceutical field, Policy, Insurance, Business Healthcare, Medical News, Health News, Pharma News, Healthcare and Investment. She has completed her B.Com from Delhi University and then pursued postgraduation in M.Com. She can be contacted at editorial@medicaldialogues.in Contact no. 011-43720751