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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

Status: Recruiting
Location: See location...
Intervention Type: Biological
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 1 month
Maximum Age: 25
Healthy Volunteers: f
View:

• Patient (age from 14 to 25 years) and/or patient's legal representative (age from 0 to 18 years) should provide written informed consent.

• Patients with one of the following disease:

‣ Acute myeloid leukemia: a. primary refractory disease (absence of complete remission (CR) after two induction regimens), b. refractory relapse (absence of CR after one salvage regimen), c. MRD-persistence before conditioning (presence of residual leukemic population more than 0,01% of bone marrow nucleated cells by flow cytometry);

⁃ Acute T-lymphoblastic leukemia: a. primary refractory disease (absence of complete remission (CR) after two induction regimens), b. refractory relapse (absence of CR after one salvage regimen), c. MRD-persistence before conditioning (presence of residual leukemic population more than 0,1% of bone marrow nucleated cells by flow cytometry);

⁃ Acute mixed phenotype leukemia: a. primary refractory disease (absence of complete remission (CR) after two induction regimens), b. refractory relapse (absence of CR after one salvage regimen), c. MRD-persistence before conditioning (presence of residual leukemic population more than 0,01% of bone marrow nucleated cells by flow cytometry).

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

• Haploidentical or matched related donor was chosen and is available for allo-HSCT (and NK-cell therapy).

• Patient's clinical status: Lansky/Karnowski index ≥50%.

• 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.

• Heart function: left ventricular ejection fraction ≥40%.

• Lung function: lung capacity ≥50%, for children who cannot carry out of respiratory function - oxygen saturation during pulse oximetry ≥92% (without supplemental oxygen).

⁃ Life expectancy ≥8 weeks.

⁃ Patients who agree to long-term follow up for up to 2 years.

Locations
Other Locations
Russian Federation
Dmitry Rogachev Federal Research and Clinical Centre of Paediatric Haematology, Oncology and Immunology
RECRUITING
Moscow
Contact Information
Primary
Timofei Y Zavidnyi, MD
timofey.zavidnyy@dgoi.ru
+79153492188
Time Frame
Start Date: 2025-05-09
Estimated Completion Date: 2027-10
Participants
Target number of participants: 15
Treatments
Experimental: Biological: Donor-derived Natural Killer Cell Infusions
Sponsors
Leads: Federal Research Institute of Pediatric Hematology, Oncology and Immunology

This content was sourced from clinicaltrials.gov

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