Leukaemia Trial, Recruiting NCT06301425 Sponsor: Peking University People's Hospital Condition: Leukaemia
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Leukaemia Trial, Recruiting

NCT06301425
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 newly diagnosed with acute myeloid leukaemia (AML)
  • People whose AML has been classified as "adverse-risk" based on a standard medical scoring system called ELN 2022 criteria (confirm with trial site)
  • People who were between 16 and 65 years old at the time of their AML diagnosis
  • People whose leukaemia went into complete remission (no detectable cancer) after 1 or 2 rounds of initial chemotherapy treatment
  • People who are largely able to carry out normal daily activities, with little to no physical limitation (rated 0 or 1 on a standard medical scale)
  • People who are willing and able to give written consent to participate, or whose legal guardian is able to do so on their behalf

Who may not be able to join:

  • People whose AML has been classified as "favourable-risk" or "intermediate-risk" under the ELN 2022 criteria, rather than adverse-risk
  • People who were younger than 16 or older than 65 at the time of their AML diagnosis
  • People whose leukaemia only went into remission after 3 or more rounds of chemotherapy, or whose leukaemia did not go into remission at all
  • People who have significant physical limitations affecting daily activity (rated 2 or higher on the standard medical scale)
  • People who have other serious illnesses or mental health conditions that could affect their safety, ability to follow the study plan, attend follow-up visits, or give informed consent

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 28 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: Xiaodong Mo, Peking University People's Hospital

Phone: 86-10-88326001

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
24 May 2024
Est. completion
1 May 2027

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Event-free survival (EFS)

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: 28 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