Leukaemia Trial, Recruiting
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.
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
Where this trial is recruiting
Primary endpoints
Event-free survival (EFS)
Can't join this trial?
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.