Clinical Trial

Peritransplant Ruxolitinib for Patients With Primary and Secondary Myelofibrosis

Active, Not Recruiting Phase 2
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Summary
This phase II trial studies how well administering ruxolitinib before, during, and after allogeneic hematopoietic stem cell transplantation works in preventing graft versus host disease and improving transplant outcomes in patients with primary and secondary myelofibrosis. Donor hematopoietic stem cell transplantation (HSCT) is currently the only treatment with proven curative potential for myelofibrosis, however, myelofibrosis patients have a high risk for developing graft versus host disease post-transplant. Graft versus host disease is a condition where the transplanted cells from a donor can attack the body's normal cells. Ruxolitinib, a janus-associated kinase (JAK) inhibitor, is known to decrease inflammatory signals, which may reduce spleen size and decrease symptoms such as night sweats and weight loss. Administering ruxolitinib before, during, and after transplant may decrease the incidence and severity of graft versus host disease, increase survival, and improve quality of life in patients with primary and secondary myelofibrosis.
Protocol Amendment History 29 amendments
This ClinicalTrials.gov record has been amended 29 times since 2020-05-08; most recent amendment 2026-04-10.
Status change: Recruiting → Active, Not Recruiting 2026-01-28
Status change: Not Yet Recruiting → Recruiting 2020-09-02
Trial Details
NCT Number NCT04384692
Lead Sponsor Fred Hutchinson Cancer Center
Conditions Primary Myelofibrosis, Secondary Myelofibrosis
Enrollment 53 participants
Start Date 2020-12-18
Primary Completion 2026-04-03 (estimated)
Study Completion 2030-04-23 (estimated)
Updated on ClinicalTrials.gov 2026-04-14