Leukemia, Acute Myeloid

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

Condition / disease
Location
Status: Not yet recruiting

Digital Patient-Reported Assessment in Older Adults With Acute Leukemia

This pilot study will evaluate the feasibility of implementing a structured digital patient-reported assessment pathway in adults aged 65 years or older with acute leukemia. Following activation of the institutional MiAsturSalud/SESPA platform, participants will complete the EORTC QLQ-C30 and FACT-Leu remotely after the baseline visit and will repeat the digital assessment at 3-6 months. The primary outcome will be completion of at least 80% of the baseline digital assessment within 7 days. Secondary outcomes will be caregiver assistance requirement, non-completion of the planned digital follow-up assessment, and elapsed completion time. The study is not designed to establish clinical efficacy.

Participants needed: 20
Trial details
Age: 65+Biological sex: AllType: InterventionalSponsor: Fundación para la Investigación Biosanitaria del Principado de AsturiasUpdated: Aug 6, 2026Locations: 1
Eligibility criteria

Age 65 years or older. [+5]

Cognitive impairment that, in the treating hematologist's clinical judgment, pre... [+2]

Status: Not yet recruiting

Revumenib, Azacitidine, and VENetoclax in Newly Diagnosed KMT2A-Rearranged AML

This study is testing a new treatment combination called RAVEN, which includes revumenib, azacitidine, and venetoclax, in patients who are newly diagnosed with a specific type of acute myeloid leukemia (AML) called KMT2A- translocated AML. People with this type of AML often have poor outcomes, so new treatments are needed that may work better and cause fewer side effects. The study has two parts: 1. Induction Phase: Patients will receive treatment for up to 3 cycles. Each cycle lasts 28 days. The goal is to help the leukemia go into remission. 2. Continuation Phase: After remission and blood count recovery, patients will continue treatment until the leukemia returns, side effects become too severe, the patient receives a stem cell transplant, or another reason to stop treatment occurs. Patients who receive an allogeneic stem cell transplant (stem cells from a donor) may also join a separate part of the study to test revumenib as maintenance treatment after transplant.

Participants needed: 88
Trial details
Phase: Phase 2Age: 18-65Biological sex: AllType: InterventionalSponsor: UNC Lineberger Comprehensive Cancer CenterUpdated: Jun 30, 2026Locations: 1
Eligibility criteria

Written informed consent obtained to participate in the study and HIPAA authoriz... [+3]

Isolated myeloid sarcoma (patients must have blood or marrow involvement with AM... [+2]

Status: Not yet recruiting

Phase I Clinical Trial of ThINKK Adoptive Immunotherapy After Allogeneic Hematopoietic Transplantation in Children With Leukemia or Neuroblastoma

A first-in-class adoptive immunotherapy we called ThINKK, for Therapeutic Inducers of Natural Killer (NK) cell Killing, have been designed for use after hematopoietic stem cell transplantation (HSCT), where the proper stimulation of graft-derived NK cells has been shown to prevent relapse. ThINKK immunotherapy builds on our earlier research on NK cells and plasmacytoid dendritic cells (PDC) in cord blood and after HSCT. PDC are the sentinels of the immune system. Upon viral nucleic acids detection, PDC secrete a vast array of chemokines and cytokines that stimulate NK cells. PDC stimulation enhances NK cells killing of infected cells that express stress-induced molecules. Cancer cells also express stress-related molecules at their surface. However, NK cells do not receive PDC stimulation when fighting cancer. ThINKK therapy is designed to provide this necessary stimulation.

Participants needed: 12
Trial details
Phase: Phase 1Age: 2-12Biological sex: AllType: InterventionalSponsor: Michel DuvalUpdated: Apr 8, 2026Locations: 2
Eligibility criteria

Between 2 and less than 13 years old at time of informed consent form signature. [+5]

Current grade 3 or 4 acute GvHD (per MAGIC criteria). [+16]