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Clinical study for donor-derived activated NK cells in the treatment of acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation for minimal residual disease recurrence

Clinical study for donor-derived activated NK cells in the treatment of acute myeloid leukemia after allogeneic hematopoietic stem cell transplantation for minimal residual disease recurrence

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1900027856
Enrollment
Unknown
Registered
2019-11-30
Start date
2019-11-30
Completion date
Unknown
Last updated
2019-12-10

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

Conditions

Blood disease

Interventions

Case series:NK cell infusion

Sponsors

Beijing Boren Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
3 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. Patients diagnosed with acute myeloid leukemia and having MRD recurrence after Allo-HSCT (US NCCN 2019.2 standard); 2. More than 3 months after allogeneic hematopoietic stem cell transplantation; 3. Hemoglobin (Hb) >=60g/L, white blood cell count (WBC) >=2.5x10^9/L, platelet count >=30x10^9/L; 4. Aged 3-70 years; 5. Patients who have failed standard treatment or have GVHD manifestations and cannot perform DLI; 6. Patients have self-knowledge ability and can sign informed and voluntary consent forms; 7. Patients or their clients, guardians of pediatric patients signed the informed and voluntary consent form and joined the study.

Exclusion criteria

Exclusion criteria: 1. Intracranial hypertension or unconsciousness; 2. Symptomatic heart failure or severe arrhythmia; 3. Respiratory; 4. With other types of malignant tumor diseases; failure; 5. T lymphocytic acute leukemia; 6. Diffuse intravascular; 7. Serum creatinine and / or urea nitrogen >=1.5 times the normal value;coagulation; 8. Serum total bilirubin >=1.5 times the normal value; 9. Sepsis or other difficult-to-control infections; 10. Uncontrollable diabetes; 11. severe mental disorders; 12. WHO physical status classification >=3; 13. People who are allergic to IL2; 14. Organ transplant recipients; 15. Pregnant and lactating women.

Design outcomes

Primary

MeasureTime frame
Bone marrow MRD;

Countries

China

Contacts

Public ContactTong Wu

Beijing Boren Hospital

wut@borenhospital.com+86 13801044860

Outcome results

None listed

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