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 are covered by a social security health scheme or an equivalent benefit program
- People who have read, understood, and signed a written consent form agreeing to take part
- People aged 60 to 74 years old who have been diagnosed with a new or secondary form of acute myeloid leukemia (AML) — a type of blood cancer — with an intermediate or high-risk genetic profile, or with a related bone marrow condition called myelodysplastic syndrome (RAEB), and whose disease has gone into complete remission (fewer than 5% abnormal cells) after initial treatment
- People who have a medical reason why they cannot receive the standard high-intensity preparation treatment used before a conventional bone marrow transplant
Who may not be able to join:
- People whose AML has been classified as standard (lower) risk based on their genetic profile
- People diagnosed with a specific type of leukemia called promyelocytic leukemia with a particular genetic change known as t(15;17)
- People with a type of AML linked to specific genetic changes known as t(8;21) or inv(16) (confirm with trial site)
- People with a normal chromosome pattern and a genetic profile considered lower risk — specifically those with certain gene markers (NPM1+, FLT3-) or a double mutation in a gene called CEBPα, or people whose chronic myeloid leukemia has progressed to a later stage called blast phase
- People who are under legal guardianship, who have had their freedoms restricted, or who have any condition that may affect their ability to understand and agree to the consent process
- People who do not wish to participate
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: Jérôme Cornillon, MD, CHU de Saint-Etienne
Phone: 04 77 91 67 26
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
Rate of overall survival
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.