Incyte Corporation Release: Jakafi® (Ruxolitinib) Continues To Show Improved Overall Survival For Patients With Myelofibrosis In Further Analyses Of Phase III Data Presented At 2013 American Society of Hematology

free biotech news Get the latest biotech news where you want it. Sign up for the free GenePool newsletter today!

NEW ORLEANS--(BUSINESS WIRE)--Incyte Corporation (Nasdaq: INCY) announced today that more than 35 analyses from clinical studies of Jakafi® (ruxolitinib) were presented at the 2013 American Society of Hematology (ASH) Annual Meeting from Dec. 7 to 10 in New Orleans. Jakafi, an oral JAK1/JAK2 inhibitor, is FDA-approved for the treatment of patients with intermediate or high-risk myelofibrosis (MF).

Help employers find you! Check out all the jobs and post your resume.

MORE ON THIS TOPIC