Karyopharm Gets FDA Fast Track Designation for Myelofibrosis Treatment
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Dow Jones
By Ben Glickman
Karyopharm Therapeutics said Monday it received Fast Track Designation from the U.S. Food and Drug Administration for its treatment for myelofibrosis.
The Newton, Mass.-based pharmaceutical company said selinexor is currently being tested in conjunction with ruxolitinib to treat a form of myelofibrosis, a rare form of blood cancer, in a Phase 3 study. The study was initiated last month.
Fast track status from the FDA is meant to speed up the development and review of treatments for serious and life-threatening conditions.
Top-line data from the Phase 3 study is expected in 2025.
Write to Ben Glickman at ben.glickman@wsj.com
(END) Dow Jones Newswires
July 17, 2023 16:33 ET (20:33 GMT)
Copyright (c) 2023 Dow Jones & Company, Inc.-
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