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Ruxolitinib in the treatment of transplantation related autoimmune cytopenia

Ruxolitinib in the treatment of transplantation related autoimmune cytopenia

Status
Recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300077788
Enrollment
Unknown
Registered
2023-11-20
Start date
2022-07-16
Completion date
Unknown
Last updated
2023-11-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

transplantation related autoimmune cytopenia

Interventions

Ruxolitinib group:Weight <25kg, 2.5mg, weight = 25kg, 5mg, take orally once or twice a day
According to the condition and tolerance, the maximum dose can be increased to 10mg/time, twice a day
Prednisone group:1-2mg/kg/d to start treatment (or equivalent hormone)

Sponsors

Medical Center of Hematology, Xinqiao Hospital of Army Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
No minimum to 70 Years

Inclusion criteria

Inclusion criteria: 1. After allogeneic transplantation, there is no limit to men and women and age; 2. Consider patients diagnosed with AIC; 3. The basic disease is stable, without progression and recurrence; 4. No active or chronic infection

Exclusion criteria

Exclusion criteria: 1.Evidence of recurrence of primary disease or recurrence after transplantation; 2.There is uncontrolled active infection;3.Severe liver and kidney dysfunction; 4.Clinically significant or uncontrolled heart disease (grade III or IV congestive heart failure); 5.Those who are allergic to lucotinib phosphate or have a more serious allergic constitution; 6.At the same time, participate in other clinical researchers.

Design outcomes

Primary

MeasureTime frame
Overall response rate after 6 months of treatment;

Secondary

MeasureTime frame
2-year overall survival;2-year disease-free survival rate;Relapse rate;Proportion of starting secondary systemic immunosuppressive therapy;Proportion of Ruxolitinib discontinued due to toxicity or intolerance;Adverse drug reactions;Lymphocyte subsets;Incidence of infection;Overall response rate after 3 months and 12 months of treatment;

Countries

China

Contacts

Public ContactChen ting

Medical Center of Hematology, Xinqiao Hospital of Army Medical University

747640395@qq.com+86 136 3792 0152

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026