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NCT07228624 · ClinicalTrials.gov registry record · Phase 2

Ruxolitinib Before, During and After Hematopoietic Cell Transplant in Older Patients With Myelofibrosis and Myelodysplastic Syndrome/Myeloproliferative Neoplasm Overlap Syndromes

A Phase 2 study of Primary Myelofibrosis and Myelodysplastic/Myeloproliferative Neoplasm, sponsored by Fred Hutchinson Cancer Center.

Recruiting
Registry status
Phase 2
Development phase
50
Enrollment target
1
Study location

NCT07228624: Recruiting Phase 2 study of Primary Myelofibrosis and Myelodysplastic/Myeloproliferative Neoplasm, sponsored by Fred Hutchinson Cancer Center.

NCT07228624 is a Phase 2 study of Primary Myelofibrosis and Myelodysplastic/Myeloproliferative Neoplasm that is actively recruiting participants, run by Fred Hutchinson Cancer Center. The registered enrollment target is 50 participants, below the 119-participant average among 30 other Primary Myelofibrosis trials with a reported enrollment target (58% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07228624, a Phase 2 study of Primary Myelofibrosis and Myelodysplastic/Myeloproliferative Neoplasm, is actively recruiting participants, sponsored by Fred Hutchinson Cancer Center.

RECRUITING
Registry status
Phase 2
Development phase
50 participants
Enrollment target
1
Study location

Study Summary

This phase II trial tests the effect of adding ruxolitinib to standard graft versus host disease (GVHD) prevention in treating older patients with myelofibrosis (MF) or myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN) overlap syndromes before, during, and after a donor (allogeneic) hematopoietic cell transplant (HCT). Allogeneic HCT is a procedure in which a person receives blood-forming stem cells (cells from which all blood cells develop) from a genetically similar, but not identical donor. Giving chemotherapy, such as cytoxan and busulfan or fludarabine and melphalan, before a donor transplant helps kill cancer cells in the body and helps make room in the patient's bone marrow for new blood-forming cells (stem cells) to grow. However, sometimes the transplanted cells from a donor can attack the body's normal cells (called GVHD). Giving standard prevention (prophylaxis) therapies, such as tacrolimus and methotrexate, after the transplant may stop this from happening. Methotrexate, a type of antifolate, is in a class of medications called antimetabolites. Methotrexate stops cells from using folic acid to make deoxyribonucleic acid and may kill cancer cells. Tacrolimus is used to help reduce the risk of rejection by the body of organ and bone marrow transplants. Ruxolitinib, a type of Janus-associated kinase (JAK) inhibitor, blocks a protein called JAK, which may help keep abnormal blood cells or cancer cells from growing. It may also lower the body's immune response and prevent the development of GVHD. Giving ruxolitinib before, during and after allogeneic HCT in addition to standard GVHD prophylaxis may be safe, tolerable and effective in preventing GVHD and improving outcomes in older patients with MF or MDS/MPN overlap syndrome.

Primary Outcome

Will be estimated as a simple proportion, and the upper bound of the one-sided 95% confidence interval for the estimated proportion will be estimated using the Clopper-Pearson method. The exact binomial test will be used to compare the observed probability to the benchmark of 65%.

Interventions

  • DRUG Cyclophosphamide
  • PROCEDURE Computed Tomography
  • DRUG Busulfan
  • DRUG Ruxolitinib
  • PROCEDURE Allogeneic Hematopoietic Stem Cell Transplantation

Study Locations (1)

Washington

  • Fred Hutch/University of Washington Cancer Consortium - Seattle

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2026-02-04
Est. Completion 2030-09-01
Phase Phase 2
Fred Hutchinson Cancer Center

483 total trials

What NCT07228624 shows while recruiting

NCT07228624 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 119-participant average among 30 other Primary Myelofibrosis trials with a reported enrollment target (58% lower).

The record links to 3 conditions, with Primary Myelofibrosis appearing as the primary indexed condition, and to 5 interventions - of which Cyclophosphamide is the first listed.

NCT07228624 reports a single indexed study location in Washington.

Frequently Asked Questions

What is clinical trial NCT07228624 about?

NCT07228624 is a clinical study titled "Ruxolitinib Before, During and After Hematopoietic Cell Transplant in Older Patients With Myelofibrosis and Myelodysplastic Syndrome/Myeloproliferative Neoplasm Overlap Syndromes". This phase II trial tests the effect of adding ruxolitinib to standard graft versus host disease (GVHD) prevention in treating older patients with myelofibrosis (MF) or myelodysplastic syndrome/myeloproliferative neoplasm (MDS/MPN) overlap syndromes before, during, and after a donor (allogeneic) hem...

What is the current status of trial NCT07228624?

This trial is currently recruiting. It is a Phase 2 study. The enrollment target is 50 participants. The study started on 2026-02-04. Estimated completion is 2030-09-01.

What conditions does trial NCT07228624 study?

This clinical trial studies the following conditions: Primary Myelofibrosis, Myelodysplastic/Myeloproliferative Neoplasm, Secondary Myelofibrosis.

What interventions are being tested in trial NCT07228624?

The interventions under investigation include: Cyclophosphamide (DRUG), Computed Tomography (PROCEDURE), Busulfan (DRUG), Ruxolitinib (DRUG), Allogeneic Hematopoietic Stem Cell Transplantation (PROCEDURE).

Who is sponsoring clinical trial NCT07228624?

This trial is sponsored by Fred Hutchinson Cancer Center, which has 483 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07228624 being conducted?

This trial has 1 study location across Washington. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Primary Myelofibrosis

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT07228624's enrollment target sits among peer trials

50 18th of 30 higher than 12 of 30 other Primary Myelofibrosis trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Primary Myelofibrosis trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT07228624, the US trial registry maintained by the National Library of Medicine. NCT07228624 (small enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.