Phase 2 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:
- The participant or their guardian must be willing to sign a written consent form agreeing to take part in the trial.
- Participants must be male or female, aged between 1 and 17 years old (inclusive).
- Participants must have been diagnosed with acute lymphoblastic leukemia (a type of blood cancer) according to World Health Organization standards.
- The leukemia must be in complete remission (meaning no signs of the disease can be detected in the blood) before the transplant takes place.
- A suitable half-matched (haploidentical) family donor must be available, and the participant or guardian must agree to proceed with this type of stem cell transplant.
- Participants must have a general health score of 70 or higher on a standard medical scale, meaning they are able to care for themselves and do normal daily activities.
- Heart function must be within an acceptable range based on a standard medical classification system (confirm with trial site).
- Liver enzyme levels (ALT and AST) must be no more than 2.5 times the normal upper limit, and bilirubin levels no more than 2 times the normal upper limit.
- Kidney function must show creatinine levels no more than 1.5 times the normal upper limit, or the kidneys must be filtering at an adequate rate (at least 60 ml/min).
- Lung function must be acceptable — meaning no significant breathing difficulties, no need for oxygen support, no lung scarring condition, and no active lung infection.
Who may not be able to join:
- People whose leukemia has not gone into complete remission before the transplant.
- People who have chosen a donor who is not a half-matched (haploidentical) family member.
- People with serious heart, liver, kidney, or lung disease that would make it unsafe to go through the pre-transplant treatment process.
- People who have an active infection that is not responding to treatment, or other life-threatening health complications.
- People with a history of another type of cancer, a psychiatric disorder, or HIV infection.
- People whose participant or guardian refuses to sign the consent form, is unwilling to attend required follow-up appointments, or does not agree to their data being used to support future research and medical practice.
- People whom the trial investigator considers unsuitable for any other reason.
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: Xiangbo Wan, PhD., The First Affiliated Hospital of Zhengzhou University
Phone: +86037166862278
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
Relapse-free survival (RFS); acute Graft Versus Host Disease (aGVHD); Overall Survival (OS)
Can't join this trial?
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.