NCT04669210 PTCy and Ruxolitinib vs PTCy, Tacrolimus and MMF in MUD and Haploidentical HSCT Status COMPLETED Phase PHASE2
NCT04603495 Phase 3 Study of Pelabresib (CPI-0610) in Myelofibrosis (MF) (MANIFEST-2) Status ACTIVE_NOT_RECRUITING Phase PHASE3
NCT04562389 Study of Selinexor in Combination With Ruxolitinib in Myelofibrosis Status ACTIVE_NOT_RECRUITING Phase PHASE3
NCT04551131 Use Of A Response-Adapted Ruxolitinib-Containing Regimen For The Treatment Of Hemophagocytic Lymphohistiocytosis Status ACTIVE_NOT_RECRUITING Phase PHASE1/PHASE2
NCT04551066 To Evaluate the Efficacy and Safety of Parsaclisib and Ruxolitinib in Participants With Myelofibrosis (LIMBER-313) Status TERMINATED Phase PHASE3
NCT04551053 To Evaluate Efficacy and Safety of Parsaclisib and Ruxolitinib in Participants With Myelofibrosis Who Have Suboptimal Response to Ruxolitinib (LIMBER-304) Status TERMINATED Phase PHASE3
NCT04543279 Fostamatinib as a Single Agent or in Combination With Ruxolitinib for Treatment of Patients With Myelofibrosis With Severe Thrombocytopenia Status TERMINATED Phase PHASE2
NCT04530344 Assess the Long Term Efficacy and Safety of Ruxolitinib Cream in Participants With Vitiligo Status COMPLETED Phase PHASE3
NCT04492618 Ruxolitinib Cream in the Treatment of Cutaneous Necrobiosis Lipoidica Status COMPLETED Phase PHASE2
NCT04485260 An Open-Label, Multicenter, Phase 1b/2 Study of the Safety and Efficacy of KRT-232 Combined With Ruxolitinib in Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera MF (Post-PV-MF), Or Post-Essential Thrombocythemia MF (Post ET-MF) Who Have a Suboptimal Response to Ruxolitinib Status UNKNOWN Phase PHASE1/PHASE2
NCT04480086 Safety and Tolerability Study of Mivebresib Tablet Alone or in Combination With Ruxolitinib Tablet or Navitoclax Tablet in Adult Participants With Myelofibrosis Status TERMINATED Phase PHASE1
NCT04472598 Study of Oral Navitoclax Tablet In Combination With Oral Ruxolitinib Tablet When Compared With Oral Ruxolitinib Tablet To Assess Change In Spleen Volume In Adult Participants With Myelofibrosis Status COMPLETED Phase PHASE3
NCT04468984 Study of Oral Navitoclax Tablet in Combination With Oral Ruxolitinib Tablet Versus Best Available Therapy to Assess Change in Spleen Volume in Adult Participants With Relapsed/Refractory Myelofibrosis Status ACTIVE_NOT_RECRUITING Phase PHASE3
NCT04455841 INCB000928 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Anemia Due to Myeloproliferative Disorders Status ACTIVE_NOT_RECRUITING Phase PHASE1/PHASE2
NCT04454658 Safety and Tolerability Study of Oral ABBV-744 Tablet Alone or in Combination With Oral Ruxolitinib Tablet or Oral Navitoclax Tablet in Adult Participants With Myelofibrosis Status ACTIVE_NOT_RECRUITING Phase PHASE1
NCT04446806 Prevention and Treatment of Differentiation Syndrome in Patients With Acute Promyelocytic Leukemia Status UNKNOWN Phase PHASE4
NCT04384692 Peritransplant Ruxolitinib for Patients With Primary and Secondary Myelofibrosis Status ACTIVE_NOT_RECRUITING Phase PHASE2
NCT04377620 Assessment of Efficacy and Safety of Ruxolitinib in Participants With COVID-19-Associated ARDS Who Require Mechanical Ventilation (RUXCOVID-DEVENT) Status TERMINATED Phase PHASE3