High Risk Acute Myeloid Leukemia

7

Review clinical trials related to High Risk Acute Myeloid Leukemia. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Recruiting

Phase 1/2: CD45RA Depleted Stem Cell Addback to Prevent Viral or Fungal Infections Post TCRab/CD19 Depleted HSCT

The major morbidities of allogeneic hematopoietic stem cell transplant (HSCT) using donors that are not human leukocyte antigen (HLA) matched siblings are graft vs host disease (GVHD) and life- threatening infections. T cell receptor alpha beta (TCRαβ) T lymphocyte depletion and CD19+ B lymphocyte depletion of alternative donor hematopoietic stem cell (HSC) grafts is effective in preventing GVHD, but immune reconstitution may be delayed, increasing the risk of infections. The central hypothesis of this study is that an addback of CD45RO memory T lymphocytes, derived from a fraction of the original donor peripheral stem cell product depleted of CD45RA naïve T lymphocytes, will accelerate immune reconstitution and help decrease the risk of infections in TCRab/CD19 depleted PSCT.

Participants needed: 100
Trial details
Phase: Phase 1, Phase 2Age: 1-25Biological sex: AllType: InterventionalSponsor: Children's Hospital of PhiladelphiaUpdated: Apr 15, 2026Locations: 1
Eligibility criteria

Disease for which allogeneic HSCT may be curative. [+5]

Patients who have performance score less than 60. [+15]

Status: Recruiting

Clinical Study to Evaluate the Safety and Efficacy of γδ T Cells for the Prevention of Relapse After Allogeneic Transplantation in Patients With High-risk Acute Myeloid Leukemia

This is an investigator-initiated clinical trial evaluating the safety and efficacy of allogeneic γδ T cell infusion for relapse prevention in high-risk acute myeloid leukemia patients after transplantation.

Participants needed: 40
Trial details
Age: 18-65Biological sex: AllType: InterventionalSponsor: Donghua ZhangUpdated: Nov 19, 2025Locations: 1
Eligibility criteria

Voluntarily signs the informed consent form and is expected to be able to comple... [+13]

Diagnosis of another malignancy within 3 years prior to screening, except for ad... [+12]

Status: Recruiting

Novel Digital Application for Patients With Acute Leukemia

This research study is evaluating to examine the efficacy of a novel a self-administered digital application (DREAMLAND) for improving patients' long-term quality of life and psychological outcomes for patients with acute myeloid leukemia undergoing intensive chemotherapy.

Participants needed: 200
Trial details
Age: 18-120Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Nov 10, 2025Locations: 3
Eligibility criteria

Hospitalized patients (age > 18 years) with a diagnosis of AML. [+2]

Patients with a diagnosis of acute promyelocytic leukemia [+1]

Status: Recruiting

Venetoclax-Enhanced BUCY vs. Standard BUCY Conditioning in High-Risk AML and MDS Patients Undergoing Allo-HSCT (Ven-BUCY Study)

This is a prospective, multicenter, randomized controlled trial designed to evaluate the efficacy and safety of venetoclax-enhanced BUCY (Ven-BUCY) conditioning compared to the standard BUCY regimen in patients with high-risk acute myeloid leukemia (AML) or myelodysplastic syndromes (MDS) undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT). Eligible participants aged 12 to 60 years will be randomized 1:1 to receive either Ven-BUCY or standard BUCY conditioning. The primary endpoint is relapse-free survival (RFS) at two years post-transplant. Secondary outcomes include overall survival, relapse rate, non-relapse mortality, measurable residual disease (MRD), and treatment-related adverse events. The study aims to improve post-transplant outcomes by deepening disease remission through the addition of venetoclax, a BCL-2 inhibitor known to target leukemia stem cells and enhance chemotherapy sensitivity.

Participants needed: 138
Trial details
Age: 12-60Biological sex: AllType: InterventionalSponsor: First Affiliated Hospital of Zhejiang UniversityUpdated: Sep 19, 2025Locations: 1
Eligibility criteria

Diagnosis of acute myeloid leukemia (AML) or myelodysplastic syndrome (MDS) acco... [+26]

Uncontrolled cardiovascular disease or New York Heart Association class III/IV h... [+8]

Status: Recruiting

Specialty Compared to Oncology Delivered Palliative Care for Patients With Acute Myeloid Leukemia

This research study is evaluating whether primary palliative care is an alternative strategy to specialty palliative care for improving quality of life, symptoms, mood, coping, and end of life outcomes in patients with acute myeloid leukemia (AML).

Participants needed: 2,300
Trial details
Age: 18-120Biological sex: AllType: InterventionalSponsor: Massachusetts General HospitalUpdated: Jul 25, 2025Locations: 20
Eligibility criteria

Patient Inclusion Criteria [+7]

Patients with a diagnosis of acute promyelocytic leukemia (APML) [+4]

Status: Not yet recruiting

Effect of Donor Chose on the Outcomes of GVHD Prophylaxis Underwent the Combined Treatment of ATG/PTCy for Haplo-HSCT

This is a prospective, multicenter, cohort study. The high-risk, relapse and refractory AML patients were enrolled in this study. And the goal of this study is to study the effect of the parous female donor and young male donor on the outcomes of graft-versus-host disease (GVHD) prophylaxis underwent the combination of ATG and PTCy for haploidentical peripheral blood stem cell transplantation

Participants needed: 114
Trial details
Age: 18-55Biological sex: AllType: ObservationalSponsor: Shanghai General Hospital, Shanghai Jiao Tong University School of MedicineUpdated: Jan 7, 2025Duration: 1 Year
Eligibility criteria

ELN prognostic stratification high-risk group (see Appendix for criteria) [+3]

Intermediate-low risk AML patients (ELN criteria); [+3]

Status: Recruiting

Study of VA Combined With HAAG Regimen in Newly Diagnosed Intermediate and High-risk AML Patients

The purpose of this study is to evaluate the efficacy and safety of VA combined with HAAG in the induction treatment of newly diagnosed acute myeloid leukemia.

Participants needed: 60
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: The First Affiliated Hospital of Soochow UniversityUpdated: May 1, 2024Locations: 1
Eligibility criteria

Newly diagnosed intermediate and high-risk AML according to the WHO (2022) class... [+7]

AML transformed with chronic myelogenous leukemia. [+9]