Eli Lilly has to wait a while longer for FDA verdict

Partners Eli Lilly and Incyte will have to wait until Q3 to find out whether the US health authorities can approve their drug Oluminant as a treatment for atopic dermatitis.


The US Food and Drug Administration (FDA) has extended the review period for Eli Lilly's application to get approval for the drug Olumiant, which treats atopic dermatitis in adults, according to an Eli Lilly press announcement.

The FDA has granted experts three more months to assess the data sets which Eli Lilly and Incyte have submitted for Olumiant, or barictinib, which is already approved in the US as an arthritis treatment.

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