LLY/INCY—Baricitinib NDA in RA delayed ≥18 months: https://finance.yahoo.com/news/lilly-incyte-baricitinib-101500123.html The FDA has indicated that a new clinical study is necessary for a resubmission in order to further characterize the benefit/risk across doses, in light of the observed imbalance in thromboembolic events that occurred during the placebo-controlled period of the RA clinical program.