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Lilly Pulls EU Approval Application For Olumiant In COVID-19

 
• By Ian Schofield

The European Medicines Agency says it does not have enough data to justify the approval of Olumiant for hospitalized COVID-19 patients. The marketing authorization application for another product, Reata’s Imbarkyd for chronic kidney disease, has also been withdrawn.  

Microscopic view of Coronavirus, a pathogen that attacks the respiratory tract. Analysis and test, experimentation. Sars. 3d render
The EMA says it cannot approve Olumiant for COVID-19 at present • Source: Shutterstock

Lilly Nederland BV has withdrawn the EU marketing authorization application (MAA) for its Janus kinase inhibitor, Olumiant (baricitinib), for use in treating adults and children with COVID-19 who require supplemental oxygen, after the European Medicines Agency said the company had not provided enough data for an approval recommendation.

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