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NCT Number: NCT07552649

Matched Sibling Allogenic Stem Cell Transplantation With Adoptive Immunotherapy With Regulatory And Conventional T Cells For High Risk Acute Myeloid Leukemia

The study is a multicentric, interventional study that evaluates the efficacy of allogeneic HLA-matched allo-HSCT consisting of myeloablative conditioning coupled with donor Treg/Tcon adoptive immunotherapy for high-risk AML patients.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Azienda Ospedaliera di Perugia - Ospedale S. Maria della Misericordia, Perugia, Italy

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Diagnosis of AML with adverse genetic mutations in Complete Remission (CR) or incomplete (i) CR according to ELN 2022 recommendations with or without MRD positivity at the time of the HSCT procedure;
  • Diagnosis of AML with intermediate genetic mutations in Complete remission (CR) or incomplete (i) CR according to ELN 2022 with MRD positivity at the time of the transplant;
  • Fitness to undergo allo-HCT with myeloablative conditioning regimens according to center policy;
  • Availability of a family HLA-matched hematopoietic stem cell donor suitable to be treated with G-CSF (10 mcg/kg/die) for a maximum of 7 days and able to tolerate 2 or more leukaphereses.
  • Age ≥ 18 and ≤ 70 years
  • ECOG ≤ 2
  • HCT-CI ≤ 4
  • Signature of the informed consent

Exclusion criteria

  • Prior allo-HSCT
  • AML with favorable genetic abnormalities
  • AML with intermediate genetic risk with MRD negativity
  • Active disease at transplant (> 5% bone marrow infiltration)
  • Availability of a haploidentical or matched unrelated donor (MUD)
  • Age < 18 years or > 70 years
  • ECOG > 2
  • Unacceptable lung, liver, kidney, and/or heart function and presence of relevant psychiatric diseases according to clinical judgment
  • Uncontrolled bacterial, viral, or fungal infections at time of enrollment
  • Pregnancy
  • No signature of the informed consent

Treatment and study plan

HSCT with Treg/Tcon adoptive immunotherapy

Biological

Purified CD34+ hematopoietic progenitor cells with Treg/Tcon adoptive immunotherapy in allogeneic cell transplantation from HLA-matched related donor

Primary outcomes

  1. Number of participants free from disease 2 years after HSCT

    Time frame: 2 years

    The primary objective of the study is to reduce the incidence of disease relapse after myeloablative conditioning regimen and Treg/Tcon adoptive immunotherapy-based allogeneic transplantation from HLA-matched donors in high-risk AML patients.

Secondary outcomes

  1. Number of participants that have reached engraftment 45 days after HSCT

    Time frame: 45 days

    The study will also evaluate the impact of allo-HSCT from HLA-matched donors with myeloablative conditioning regimen and Treg/Tcon adoptive immunotherapy on full donor type engraftment

  2. Number of participants that developed grade ≥ 2 acute GvHD

    Time frame: 100 days

    The study will also evaluate the impact of allo-HSCT from HLA-matched donors with myeloablative conditioning regimen and Treg/Tcon adoptive immunotherapy on grade ≥ 2 acute GvHD

  3. Number of participants free from chronic GvHD 2 years after HSCT

    Time frame: 2 years

    The study will also evaluate the impact of allo-HSCT from HLA-matched donors with myeloablative conditioning regimen and Treg/Tcon adoptive immunotherapy on chronic GvHD

  4. Number of participants who died for transplant related mortality after HSCT

    Time frame: 2 years

    The study will also evaluate the impact of allo-HSCT from HLA-matched donors with myeloablative conditioning regimen and Treg/Tcon adoptive immunotherapy on non relapse mortality (NRM)

  5. Number of patients free from ≥ 2 acute GvHD and/or moderate/severe chronic GvHD and/or relapse

    Time frame: 2 years

    The study will also measure grade ≥ 2 acute GvHD and/or moderate/severe chronic GvHD/Relapse-free survival (GRFS)

  6. Number of patients free from moderate/severe chronic GvHD and relapse

    Time frame: 2 years

    The study will also measure moderate/severe chronic GvHD-Relapse-free survival (CRFS)

  7. Number of patients alive after 2 years after allogeneic transplant

    Time frame: 2 years

    Overall survival (OS) of patients treated with allogeneic transplant

Study contacts

Contact information is provided by the study sponsor or research team.

Antonio Pierini

CONTACT

[email protected]

+39 075 578 4147

Sponsors and collaborators

Lead sponsor

Antonio Pierini

Other

Registry information

Official study title

MATCH-Treg: Matched Sibling Allogenic Stem Cell Transplantation With Adoptive Immunotherapy With Regulatory And Conventional T Cells For High Risk Acute Myeloid Leukemia

Acronym: MATCH-Treg

Important dates

Study start
2026
Primary completion
2028
Study completion
2030
First posted
Apr 27, 2026
Registry last updated
Apr 27, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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