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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

Official title: Phase I/II Clinical Trial of mbIL21 ex Vivo-expanded Donor-derived NK-cell Infusions With Hematopoietic Stem Cell Transplantation for Disease Relapse Prophylaxis in Pediatric and Young Adult Patients With Chemorefractory or Minimal Residual Disease Positive Acute Leukemia

Is NCT07256210 recruiting? Yes, currently enrolling (Oct 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 Oct 2026Location: Russia

Treatment: Donor-derived Natural Killer Cell — This 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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