New combo aims to tame Graft-Versus-Host disease in older blood cancer patients
NCT ID NCT07228624
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This phase 2 trial tests whether adding the drug ruxolitinib to standard care can prevent graft-versus-host disease (GVHD) in older patients with myelofibrosis or MDS/MPN overlap syndromes who receive a donor stem cell transplant. About 50 participants will get ruxolitinib before, during, and after the transplant, along with chemotherapy and standard GVHD prevention. The main goal is to see if this approach lowers the rate of moderate-to-severe GVHD compared to historical results.
What this could mean
Our plain-language read of the trial. This is informational only โ not medical advice or a prediction.
- Active substance
- Ruxolitinib (a JAK inhibitor drug) given before, during, and after a donor stem cell transplant
- What this could lead to
- If it works, this could reduce the risk of graft-versus-host disease and improve outcomes for older patients with myelofibrosis or related blood cancers.
- What could go wrong
- This is a small, early-phase trial (50 participants) with no guarantee of success. Adding ruxolitinib may increase side effects or fail to prevent GVHD better than standard care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Fred Hutch/University of Washington Cancer Consortium
RECRUITINGSeattle, Washington, 98109, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a Dual-Action pill tame bone marrow tumors?
- Can a new pill shrink the spleen in myelofibrosis?
- Can a daily pill shrink the spleen in myelofibrosis?
- Could a platelet-boosting drug shorten recovery after stem cell transplants?
- Can a modified interferon rein in early myelofibrosis?
- Can a drug free myelofibrosis patients from frequent blood transfusions?