Leukaemia Trial, Recruiting NCT07500441 Sponsor: Peking University People's Hospital Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT07500441
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 acute myeloid leukemia (AML).
  • People who are receiving a stem cell transplant from a donor (called an allogeneic stem cell transplant) at the hospital running this trial.
  • People whose AML does not involve certain specific genetic changes (known as fusion genes) that are routinely tested for in the laboratory — such as AML1::ETO, BCR::ABL1, and several others (confirm with trial site for the full list).
  • People for whom genetic sequencing test results (called NGS results) from the time of their original AML diagnosis are available and can be reviewed.
  • People whose AML did not involve a genetic change called an NPM1 mutation at the time of first diagnosis.
  • People whose AML showed certain gene mutations at the time of first diagnosis — such as mutations in genes like DNMT3A, TET2, ASXL1, SRSF2, or similar genes linked to blood cell changes (confirm with trial site for the full list).

Who may not be able to join:

  • People whose genetic mutation profile is not suitable for designing a specialised personalised laboratory test (called digital PCR) that is sensitive enough to detect very small amounts of disease (confirm with trial site).
  • People who do not have any measurable genetic markers in their AML that could be tracked over time to monitor whether disease remains or returns.

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 21 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.

Contact this trial

Principal Investigator: Ya-zhen Qin, Ph.D, Peking University People's Hospital

Phone: +861088324637

Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.

GP referral letter

Print a one-page summary to share with your doctor.

Trial details

Status
Recruiting
Phase
Not Applicable
Sponsor
Peking University People's Hospital
Registry
ClinicalTrials.gov
Start date
20 March 2026
Est. completion
31 December 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Cumulative Incidence of Relapse (CIR)

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: 21 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