JAKAFI® (Ruxolitinib) April 1, 2022April 1, 2022 RR FDA Approvals General Medical Oncology & Hematology The FDA on September 22, 2021 approved JAKAFI® (Ruxolitinib) for chronic Graft-Versus-Host Disease (cGVHD) after failure of one or two lines of systemic therapy in adult and pediatric patients 12 years and older. JAKAFI® is a product of Incyte Corp. Related Posts:JAKAFIĀ® (Ruxolitinib)JAKAFIĀ® (Ruxolitinib)FDA Approves JAKAFIĀ® for Acute GVHDRuxolitinib for Myelofibrosis ā An Update of Its…Long Term Data Confirms Durable Efficacy and Safety…Results of a prospective, randomized, open-label…