Acute Myeloid Leukemia in Children

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

Condition / disease
Location
Status: Recruiting

Study of the Medullary Microenvironment in Acute Childhood Leukemia

Acute leukemia (AL) is the most common cancer in children. Despite the optimization of chemotherapy treatments and the development of supportive care, a certain number of LAs relapse and/or progress to death of the child. It therefore seems essential to try to better understand the physiopathology and the mechanisms of resistance to treatment of these diseases.

Participants needed: 40
Trial details
Age: 1-15Biological sex: AllType: InterventionalSponsor: University Hospital, ToursUpdated: Nov 24, 2025Locations: 3
Eligibility criteria

Child with acute lymphoblastic or myeloblastic leukemia at diagnosis [+10]

Patient under 1 year old and over 15 years old. [+11]

Status: Recruiting

CHIP-AML22/Quizartinib: Quizartinib + Chemotherapy in Newly Diagnosed Pediatric FLT3-ITD+ and NPM1wt AML Patients

The CHIP-AML22 Master protocol has the overall aim of increasing the cure rate in newly diagnosed pediatric de novo AML patients, while avoiding unnecessary toxicity. The linked Quizartinib trial (CHIP-AML22/Quizartinib) is a phase II, single arm, open label, study on the safety, efficacy, pharmacokinetics and pharmacodynamics of quizartinib in combination with chemotherapy and as single-agent after high dose therapy in newly diagnosed pediatric AML patients with a FLT3-ITD mutation and NPM1 wild-type.

Participants needed: 60
Trial details
Phase: Phase 2Age: 1-18Biological sex: AllType: InterventionalSponsor: Princess Maxima Center for Pediatric OncologyUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

Performance status Karnofsky performance status score of >50% for subjects >16 y... [+3]

Patients with only extramedullary disease [+11]

Status: Recruiting

CHIP-AML22/Master: An Open Label Complex Clinical Trial in Newly Diagnosed Pediatric de Novo AML Patients

The CHIP-AML22 Master protocol has the overall aim of increasing the cure rate in newly diagnosed pediatric de novo AML patients, while avoiding unnecessary toxicity.

Participants needed: 905
Trial details
Phase: Phase 3Age: 1-18Biological sex: AllType: InterventionalSponsor: Princess Maxima Center for Pediatric OncologyUpdated: Aug 5, 2025Locations: 1
Eligibility criteria

Newly diagnosed AML as defined by the diagnostic criteria in section 8.1. Note t... [+7]

Previous chemotherapy or radiotherapy. This includes patients with therapy-relat... [+13]

Status: Recruiting

Individualized Treatment of Pediatric R/R AML Based on Transcriptomic Profile and in Vitro Drug Sensitivity Test

Acute myeloid leukemia (AML) accounts for about 15% to 20% of childhood leukemia, but the death rate accounts for about 50%. About 20-30% of children with AML did not achieve complete response (CR) after 2 induction treatments, and about 30% of children with CR had relapse within 3 years (including recurrence after hematopoietic stem cell transplantation).Relapsed/refractory (R/R) AML is a major cause of treatment failure and refractory survival. Reinduction chemotherapy for R/R-AML to obtain CR again, followed by hematopoietic stem cell transplantation, is the current treatment. At present, there is no recognized reinduction protocol, and the reinduction remission rate of R/R-AML varies greatly among different treatment regimens, ranging from 23 to 81%. Current guidelines recommend a new combination chemotherapy regimen consisting of new drugs without cross-resistance. This method selects sensitive chemotherapeutic drugs, and then forms a new combination chemotherapy regimen according to the characteristics of drugs, which is the choice of R/R-AML reinduction therapy.This study intends to conduct a clinical study on the individualized treatment of R/R AML patients through in vitro drug sensitivity test combined with patient transcriptomic characteristics.

Participants needed: 60
Trial details
Age: Up to 18Biological sex: AllType: InterventionalSponsor: The Children's Hospital of Zhejiang University School of MedicineUpdated: Jul 3, 2024Locations: 1
Eligibility criteria

Not listed