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www.fdanews.com/articles/138974-fda-accepts-nda-filing-for-ruxolitinib-as-a-treatment-for-myelofibrosis

FDA Accepts NDA Filing for Ruxolitinib as a Treatment for Myelofibrosis

August 4, 2011
Incyte announced that the FDA has accepted for filing the new drug application (NDA) for Incyte’s lead investigational compound, ruxolitinib, as a potential treatment for patients with myelofibrosis (MF).
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