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Study identifier: NCT06885476 Synced from ClinicalTrials.gov · July 28, 2026
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Infusion of Alloreactive nk Cells for Mrd-positive Aml Patients

Condition: Acute Myeloid Leukemia · Minimal Residual Disease · Natural Killer Cell  ·  Sponsor: IRCCS Azienda Ospedaliero-Universitaria di Bologna

PhaseNA
Planned participants22
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

This is a interventional, transplantation study. The procedure under study is the infusion of alloreactive NK cells in adult AML patients, eligible for ASCT, who achieved CR after conventional chemotherapy, but harbor MRD-positivity. Haploidentical KIR-L mismatched donors will be included if present at least one allele mismatch at a class I locus among the following ones: HLA-C alleles with Asn77-Lys80, HLA-C alleles with Ser77-Asn80, HLA-Bw4 alleles. KIR-L mismatched donor alloreactive NK cell repertoire will be evaluated in order to determine the functional cell dose to be used for NK cell collection. Phenotypical analysis of KIRs will be correlated to functional tests. NK cells will be selected from a steady-state large volume leukapheresis product from a suitable haploidentical KIR-ligand incompatible donor. NK cell purification will be performed if the donor leukapheresis product contains at least 10x106 NK cells/Kg. Immunomagnetic enrichment of NK cells will follow two subsequent steps: 1) depletion of CD3+ T cells followed by 2) positive selection of CD56+ NK cells. Patients will receive immunosuppressive chemotherapy, fludarabine (Flu) 25 mg/mq/ from day -5 to -3 and cyclophosphamide (Cy) 2 g/mq on day -2 (Flu/Cy). Two days after Cy administration, patients will be infused intravenously with a single dose of cryopreserved NK cells (day 0), which will be followed by subcutaneous administration of IL-2 (10 x 106 IU/day, 3 times weekly) for 2 weeks (6 doses total). PB…

This description comes directly from the study's public registry record.

Talk to the study team

Antonio Curti  ·  +390512144074  ·  antonio.curti2@unibo.it

Always discuss trial participation with your own doctor first.

Locations (1)

Antonio CurtiBologna, BO, ItalyRecruiting

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Source record: clinicaltrials.gov/study/NCT06885476