Clinical Study of CLL-1 CAR-T in the Treatment of Children With R/R AML
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: CAR-T.
- Who it may be relevant to
- Registry conditions: AML (Acute Myeloid Leukemia), CAR-T. Basic parameters: 3 years — 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- Center list to be confirmed — check the primary protocol.
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
A Single-Center Clinical Study Evaluating the Safety and Preliminary Efficacy of CLL-1 CAR-T in the Treatment of Children With Relapsed/Refractory Acute Myeloid Leukemia
Overview
A study to evaluate the safety and preliminary efficacy of CLL-1-targeted CAR-T cell therapy in children aged 3 to 18 years with relapsed or refractory acute myeloid leukemia (r/r AML).
Detailed description
It's a single-center, single-arm, investigator-initiated clinical study. After thorough consideration and signing of the informed consent form by the subject and/or their legal guardian(s), subjects meeting the eligibility criteria during the screening period will provide blood samples for CAR-T manufacturing. Following lymphodepleting chemotherapy, CAR-T cell infusion will be administered on D0.
Interventions
- Biological CAR-T
A infusion of CLL-1 CAR-T cells following a lymphodepleting chemotherapy regimen.
Primary outcome measures
- Incidence of Treatment-Related Adverse Events [Time frame: Up to 2 years.]
Secondary outcome measures (6)
- Overall Response Rate [Time frame: Up to 2 years.]
- Duration of Response [Time frame: Up to 2 years.]
- Relapse-Free Survival [Time frame: Up to 2 years.]
- Event-Free Survival [Time frame: Up to 2 years.]
- Overall Survival [Time frame: Up to 2 years.]
- Proportion of CLL-1-Positive Tumor Cells [Time frame: Up to 2 years.]
Eligibility criteria
Inclusion criteria
- Voluntarily sign the ICF and are expected to complete the study's follow-up examinations and procedures.
- Aged 3 to 18 years (inclusive), and body weight ≥10 kg.
- Diagnosis of AML according to the 2016 WHO classification, meeting the diagnostic criteria for relapse and refractoriness as per the "Chinese Guidelines for Diagnosis and Treatment of Relapsed/Refractory Acute Myeloid Leukemia (2017 Edition)", and currently having no clinically relevant treatment options or suitable registered clinical trials available.
- Confirmation of CLL-1 expression ≥50% on AML blasts by flow cytometry.
- Recovery from toxicities of prior therapies.
- Karnofsky score (for age ≥16 years) ≥70 or Lansky score (for age <16 years) ≥50 at screening, and an expected survival >3 months.
- Suitable function of the liver, kidneys, hematological system, lungs and heart is required.
- Females subjects of childbearing potential must have a negative blood pregnancy test at screening and agree to use effective contraception during the study and within 1 year after the last dose of study drug.
- Male subjects with reproductive potential must agree to use barrier contraception or practice complete abstinence until 1 year after the last study treatment.
- Eligible blood cell specimen can be provided.
Exclusion criteria
- Diagnosis of APL.
- History of other malignancies within 3 years prior to screening, except for adequately treated carcinoma in situ of the cervix, papillary thyroid carcinoma, basal cell or squamous cell skin cancer, localized prostate cancer treated with radical surgery, and ductal carcinoma in situ treated with radical surgery.
- Evidence of CNS involvement or cranial nerve pathology.
- Subjects with active infections such as hepatitis B, hepatitis C, etc., are to be excluded.
- Subjects with a history of severe allergies or known allergy to any drug component included in this study are to be excluded.
- Subjects with severe cardiac diseases, refractory hypertension, active neurological autoimmune or inflammatory diseases, clinically significant active cerebrovascular disease, oncologic emergencies requiring urgent intervention, acute or chronic GVHD, or any uncontrolled infections requiring antibiotic therapy, etc., are unsuitable for enrollment.
- Previous organ transplant or planned organ transplant (except for hematopoietic stem cell transplantation).
- Received allo-HSCT within 6 weeks prior to screening.
- Subjects who have recently undergone major surgery or plan to undergo major surgery, excluding diagnostic procedures and biopsies.
- Subjects with severe mental disorders, alcoholism, or drug abuse.
- Subjects who, in the judgment of the investigator, have other conditions that make them unsuitable for enrollment.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- N/A
- Model
- Single group
- Masking
- Open label
- Primary purpose
- Treatment
Study locations
Center list to be confirmed — check the primary protocol.
Identifiers
NCT: NCT07338357 · BG-CT-25-012