INCYTE CORPORATION (NASDAQ:INCY) Files An 8-K Other EventsItem 8.01 Other Events.
On April 14, 2017, Eli Lilly and Company and Incyte Corporation announced that the U.S. Food and Drug Administration (“FDA”) has issued a complete response letter for the New Drug Application of the investigational medicine baricitinib, a once-daily oral medication for the treatment of moderate-to-severe rheumatoid arthritis.
The letter indicates that the FDA is unable to approve the application in its current form. Specifically, the FDA indicated that additional clinical data are needed to determine the most appropriate doses. The FDA also stated that additional data are necessary to further characterize safety concerns across treatment arms. The companies disagree with the FDA’s conclusions. The timing of a resubmission will be based on further discussions with the FDA.