www.fdanews.com/articles/177306-fda-grants-incytes-jakafi-breakthrough-therapy-designation
FDA Grants Incyte’s Jakafi Breakthrough Therapy Designation
June 29, 2016
Incyte’s Jakafi has secured breakthrough therapy designation for treatment of patients with acute graft-versus-host disease, the Wilmington, Del.-based company announced last week.
Jakafi is indicated to treat people with polycythemia vera who aren’t responsive to hydroxyurea, as well as people with intermediate or high-risk myelofibrosis.
Currently, there are no approved treatments for patients with acute GVHD.