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OncoMatch/Clinical Trials/NCT07256210

Feasibility and Safety of Donor-derived NK-cell Infusions for Leukemia Relapse Prophylaxis After Hematopoietic Stem Cell Transplantation

Is NCT07256210 recruiting? Yes, currently enrolling (Jun 2026). This Phase 2 trial studies Donor-derived Natural Killer Cell for acute myeloid leukemia.

Phase 2RecruitingFederal Research Institute of Pediatric Hematology, Oncology and ImmunologyNCT07256210Data as of Jun 2026Location: Russia

Treatment: Donor-derived Natural Killer CellThis pilot clinical trial aims to evaluate the feasibility, adverse reactions and maximum tolerated dose of mbIL21 ex vivo-expanded donor-derived NK-cell infusions before and after haploidentical or matched-related hematopoietic stem cell transplantation in a cohort of pediatric and young adult patients with chemorefractory or minimal residual disease (MRD) positive acute leukemia.

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Extracted eligibility criteria

Treatments studied

Other

Donor-derived Natural Killer Cell

Cancer type

Acute Myeloid Leukemia

Acute Lymphoblastic Leukemia

Demographics

Ages 0–25

Prior therapy

Must have received: hematopoietic stem cell transplant — indicated to receive

Patient is indicated to receive allo-HSCT according to actual clinical practice

Cannot have received: cellular therapy including allo-HSCT

Cellular therapy including allo-HSCT within prior 4 months period

Lab requirements

Kidney function

clearance of endogenous creatinine or glomerular filtration rate according to schwarz equation ≥50 ml/min/1,73 m2

Liver function

total bilirubin ≤3 uln except for gilbert's disease, alt/ast ≤3 uln

Cardiac function

left ventricular ejection fraction ≥40%

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07256210 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior cellular therapy including allo-HSCT disqualifies patients from enrollment.

Is there an age limit?

Yes. Patients must be 25 years or younger and at least 0 years old.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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