Haploidentical stem cell transplantation for myelofibrosis
Official title: Haploidentical Hematopoietic Stem Cell Transplantation for the Treatment of Myelofibrosis: A Prospective, Single-center Study
Run by Peking University People's Hospital · NCT06674382 · Data updated 2026-11-12
This study is testing a new type of stem cell transplant for people with myelofibrosis to see if it can help those who don’t have a matched donor and improve their chances of recovery.
Quick facts
| Study type | Interventional |
|---|---|
| Sex | All |
| Enrollment | 39 (estimated) |
| Sponsor | Peking University People's Hospital Academic / other |
| Drugs / interventions | ruxolitinib |
| Locations | 1 site (Beijing) |
| Status | Recruiting |
| Started | January 1, 2024 |
| Main results expected | December 31, 2027 |
| Study ends | December 31, 2027 |
| Registry record updated | September 14, 2026 |
| Trial ID | NCT06674382 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates for this study are patients diagnosed with myelofibrosis who do not have a matched sibling or unrelated donor but have access to a haploidentical donor.
✕Probably not a fit
Patients with active infections, very poor performance status, or those with an estimated survival time of less than 30 days may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This clinical trial investigates a novel haploidentical stem cell transplantation protocol for patients with myelofibrosis, a condition characterized by bone marrow failure and a high risk of leukemia. The study aims to improve outcomes for patients who do not have access to matched donors, as haploidentical donors are more readily available. By evaluating the effectiveness of this new transplantation approach, the trial seeks to address the challenges associated with graft failure and treatment-related mortality. The research is designed to provide a potential cure for myelofibrosis, which currently lacks effective treatment options.
Why it matters
Potential benefit: If successful, this approach could provide a curative treatment option for patients with myelofibrosis who lack matched donors.
How similar studies have gone: While haploidentical transplantation has shown promise in treating leukemia, its application in myelofibrosis is less studied, making this approach relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Primary disease type: Myelofibrosis (including primary myelofibrosis and myelofibrosis secondary to polycythemia vera or essential thrombocythemia). * No matched sibling donor or unrelated donor, with the availability of a haploidentical donor. * Signed informed consent. Exclusion Criteria: 1. Active infection 2. Very poor performance status (ECOG score \> 2) 3. Estimated survival time \< 30 days 4. Patient or family unable to cooperate 5. Considered unsuitable after discussion
Where it's running
-
Peking University People's Hospital
Beijing, China Recruiting
Study contacts
- Study coordinator: Sun Yuqian
- Email: sunyuqian83@hotmail.com
- Phone: 861088326666
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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MPN PROGRESSion Registry — tracking symptoms, treatments, and disease progression in people with MPNs.
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Nelfinavir to improve anemia in people with myelofibrosis by restoring iron delivery to the bone marrow
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This project will collect health, treatment, and quality-of-life information from people in Germany with primary or secondary myelofibrosis and anemia to see how their care and symptoms change over time.
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Evaluating DISC-0974 for treating anemia in myelofibrosis patients
This study tests if a new treatment called DISC-0974 can help people with myelofibrosis who have anemia feel better and improve their condition.
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Elritercept vs. placebo for adults with myelofibrosis and anemia on ruxolitinib
This study tests whether elritercept can improve anemia in adults with myelofibrosis who are taking ruxolitinib, compared with placebo.
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TQ05105 tablets for intermediate/high-risk myelofibrosis
This phase 2 study tests TQ05105 tablets to see if they help people with intermediate or high-risk myelofibrosis who have not benefited from prior JAK inhibitors.
How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.