Phase 3 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:
- You have been diagnosed with a specific type of blood cancer called AML (but not the subtype called acute promyelocytic leukemia), as defined by current medical guidelines
- Your AML is classified as high-risk or intermediate-risk and is in first remission, OR your AML is in second remission regardless of risk level (partial remission may also be considered)
- You are planned to receive a stem cell transplant from a closely matched related or unrelated donor, or from a half-matched family donor using a specific type of stem cell collection
- Your planned pre-transplant treatment meets a certain intensity threshold (confirm with trial site)
- Your planned anti-rejection medication after transplant is based on a drug called tacrolimus
- You are between 18 and 75 years old
- You are in good general health and able to carry out everyday activities with little or no limitation (as measured by a standard medical scale)
Who may not be able to join:
- You are planned to use certain other anti-rejection medications, including cyclosporine, ATG, alemtuzumab, or abatacept
- You have been found to have a specific eye condition called macular edema during the screening process
- You have significant problems with your heart, lungs, liver, or kidneys
- Your liver is not functioning well enough, based on specific blood test results being too high
- Your kidneys are not filtering blood well enough, based on a standard calculation of kidney function
- You have diabetes
- You have a current or past history of an eye inflammation condition called uveitis
- You have a current or past history of macular edema (a swelling in the eye)
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: Marcos DeLima, MD, The Ohio State University Comprehensive Cancer Center
Phone: +33 (0) 6 40 91 26 76
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)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 19 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.