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FDA tells Eli Lilly it can quickly refile NDA for hopeful Baricitinib

Discussion in 'Eli Lilly' started by RobertPhillips900, Aug 30, 2017 at 10:09 AM.

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  1. RobertPhillips900

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    Lilly will resubmit the New Drug Application for rheumatoid arthritis medication baricitinib, to the U.S. Food and Drug Administration (FDA), before the end of January 2018. The companies anticipate the FDA will classify the application as a Class II resubmission, which will start a new six-month review cycle. http://alph.st/b283c853