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:
- People who have been diagnosed with acute leukemia.
- People whose acute leukemia is complex or hard to treat — for example, those whose leukemia did not go into remission after 2 rounds of standard treatment, those who relapsed within 6 months of first remission, those who relapsed after 6 months but whose original treatment no longer worked, or those who have had a relapse at any point.
- People whose previous cancer treatments were finished at least 2 weeks ago (or 5 half-lives of the drug, whichever is shorter), with a longer gap required for certain immune-based treatments such as ipilimumab (confirm with trial site).
- People whose side effects from past cancer treatments have settled down to a mild level (grade 1 or lower), apart from minor issues like hair loss.
- People aged 15 to 64 years old.
- People with a general health and activity level rated between 0 and 3 on the ECOG scale, which measures how much a person's illness affects their daily life (confirm with trial site).
- People who do not have an active, uncontrolled infection or graft-versus-host disease (a complication that can occur after bone marrow or stem cell transplants).
- People whose doctors estimate they have a life expectancy of at least 3 months.
- People whose kidneys, liver, lungs, and heart are functioning well enough to meet specific medical thresholds — including kidney filtration rate, liver enzyme levels, heart pumping strength, blood oxygen levels, and no significant fluid around the lungs or heart (confirm with trial site for exact values).
- Women who are capable of becoming pregnant must have a negative pregnancy test before joining.
Who may not be able to join:
- People who have had another type of cancer in the past, unless they have been cancer-free for at least 3 years (some skin cancers and early-stage cancers may be assessed differently — confirm with trial site).
- People who have an active infection (fungal, bacterial, viral, or other) that is uncontrolled or suspected to be uncontrolled.
- People who have a known HIV infection.
- People with a known history of active hepatitis B or hepatitis C, unless specific blood test results show the virus is not active in the blood (confirm with trial site).
- People who have or have had a neurological or brain-related condition, such as seizures, stroke, dementia, or a brain-related autoimmune disease.
- People with serious heart conditions, such as uncontrolled irregular heartbeat, heart failure, or a heart attack within the past 6 months, or moderate to severe heart disease as classified by medical guidelines.
- People who have had a heart attack, heart procedure, stent placement, or unstable chest pain within the 12 months before joining.
- People whose cancer is growing so quickly that emergency medical treatment is likely to be needed within 6 weeks.
- People with a primary immune deficiency (a condition where the immune system does not work properly from birth or early life).
- People who have had a serious blood clot in a vein or the lungs within the past 6 months.
- People with any other medical condition that might affect the safety of the treatment or the accuracy of the study results.
- People who have had a severe allergic reaction to any of the drugs used in this study.
- People who have received a live vaccine within 6 weeks before starting the treatment preparation phase.
- Women who are pregnant or breastfeeding.
- People who are not willing or able to use effective contraception from the time of signing consent until 6 months after completing treatment.
- People who, in the opinion of the study doctor, may have difficulty completing all required visits, procedures, or follow-up appointments.
- People who have had autoimmune diseases causing organ damage (such as Crohn's disease, rheumatoid arthritis, or lupus), or who need ongoing immunosuppressive medication to manage a systemic condition.
- People who are currently participating in another clinical trial at the same time.
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: Hai Yi, Ph.D, The General Hospital of Western Theater Command
Phone: 0086-28-86571279
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
Number of Adverse Events; Overall response rate (ORR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 16 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.