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Study for chidamide and descitabine plus interferon in the treatment of early relapse of acute leukemia post hematopoietic stem cell transplantation

The treatment with chidamide and descitabine plus interferon on early relapse post hematopoietic stem cell transplantation in acute leukemia

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2000032330
Enrollment
Unknown
Registered
2020-04-26
Start date
2020-01-01
Completion date
Unknown
Last updated
2020-04-27

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

Conditions

acute leukemia

Interventions

1:Chidamide and descitabine plus interferon

Sponsors

Sichuan Academy of Medical Sciences Sichuan Provincial People's Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
7 Years to 59 Years

Inclusion criteria

Inclusion criteria: 1. Patient with acute leukemia treating by allo-HSCT; 2. MRD was detected re-positive and bone morrow test still CR after allo-HSCT.

Exclusion criteria

Exclusion criteria: 1. lactation, and unwilling to use contraception childbearing age woman; 2. patient with history of clinical significant extended QTc interval; Patients with ventricular tachycardia (VT), atrial fibrillation (AF), heart block, myocardial infarction (MI) attack within 1 year, congestive heart failure (CHF), and symptomatic coronary heart disease requiring medication; 3. Ultrasound B showed that the width of the fluid dark region of the pericardial lumen at the end of diastolic period was >=10mm; 4. Receive an organ transplant; 5. In the 7 days before enrollment, received symptomatic treatment against the previous bone marrow toxicity; 6. With active hemorrhage; 7. With disease or history of thrombus, embolism, cerebral hemorrhage, cerebral infarction, etc.; 8. Active infection, or fever that persists for 14 days prior to enrollment; 9. With HBV, HCV, HIV active infection; 10. No more than 6 weeks after main organ surgery; 11. Liver, renal function abnormal; 12. Mental disorder; unable to obtain a informed consent; 13. Drug and long-term alcohol abuse may affect the evaluation of the experimental results; 14. Leukemia infects the central nervous system; 15. Investigator judges those not suitable for involving.

Design outcomes

Primary

MeasureTime frame
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Countries

China

Contacts

Public ContactHuang Xiaobing

Sichuan Academy of Medical Sciences Sichuan Provincial People's Hospital

huangxiaobing@med.uestc.edu.cn+86 18981838236

Outcome results

None listed

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