Leukaemia Trial, Recruiting NCT06458244 Sponsor: Ruijin Hospital Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT06458244
Recruiting Not Applicable

Who may be able to join

AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI

Who might be able to join this trial:

  • People who have been diagnosed with a specific type of acute myeloid leukaemia (AML) called core-binding factor AML (CBF-AML), confirmed through genetic or chromosome testing showing particular gene fusions
  • People whose leukaemia has certain high-risk gene changes, complex chromosomal patterns, or whose disease was still detectable through specialised testing (MRD) after two rounds of chemotherapy
  • People whose diagnosis has been thoroughly assessed and confirmed as CBF-AML — not a transformed or treatment-related form of AML
  • People aged 18 to 64 years old
  • People whose liver and kidney function results fall within acceptable ranges (blood bilirubin, liver enzymes, and creatinine levels must meet specific thresholds)
  • People with normal heart function, based on heart scans and a standard heart function classification (confirm with trial site)
  • People who have a general physical fitness score of 0, 1, or 2 on a standard scale used by doctors to assess overall health (ECOG score)
  • People whose white blood cell count was below a certain level at diagnosis and who have not received any chemotherapy beforehand, except for a specific tablet called hydroxyurea
  • People whose white blood cell count was at or above a certain level at diagnosis and who have only received hydroxyurea or a specific chemotherapy drug (cytarabine) beforehand
  • Women who are not pregnant and not breastfeeding
  • Women of childbearing age who have had a pregnancy test to confirm they are not pregnant
  • People (or their family members) who have signed a form giving informed consent to participate

Who may not be able to join:

  • People whose AML developed from another blood condition (MDS), or whose AML was caused by previous cancer treatment, or who have a mixed-cell type of leukaemia, or who had leukaemia spread to the nervous system or other areas outside the bone marrow at the time of diagnosis
  • People whose AML has come back after a previous remission (relapsed AML)
  • People who have a known allergy or medical reason to avoid any of the drugs used in this trial
  • People whose liver or kidney function results fall outside the acceptable ranges for this trial
  • People with certain heart conditions, including reduced heart pumping function, significant heart failure, fluid around the heart, a recent heart attack within the past six months, or an abnormal heart rhythm reading on an ECG (confirm with trial site for specific thresholds)
  • People with certain lung conditions, including fluid on the lungs or around the lungs above a certain severity level
  • People who currently have another type of cancer in another part of the body
  • People who have active hepatitis A, B, or C, active tuberculosis, or who are HIV-positive
  • People who have other blood disorders unrelated to their leukaemia, including certain clotting problems
  • People who are unable to understand or follow the requirements of the study
  • People who are already taking part in another clinical trial, or who have any other condition that would make participation in the study unsuitable

Important: Always verify eligibility with the trial site directly before applying.

Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 2 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

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Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Registry
ClinicalTrials.gov
Start date
21 September 2024
Est. completion
20 September 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

disease-free-survival; The relation of CBF-AML genetics subgroup with MRD negativity rate after chemotherapy and DFS after transplantation

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 2 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov