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 18 years of age or older at the time of signing the consent form
- People who have been diagnosed with Acute Myeloblastic Leukaemia (a type of blood cancer), confirmed through laboratory testing, and classified according to the ELN 2022 guidelines
- People who are about to start treatment with a combination of two medicines — venetoclax and azacitidine — for the first time (note: adding a third targeted medicine to this combination is not permitted in this trial)
- People who are willing and able to read, understand, and sign a voluntary consent form before any trial procedures begin
- People who are enrolled in, or covered by, a social security system
Who may not be able to join:
- People diagnosed with a specific subtype of leukaemia called acute promyelocytic leukaemia (APL, also known as AML3)
- People whose leukaemia is considered suitable for intensive chemotherapy
- People who have previously been treated with venetoclax and/or azacitidine
- People who are currently taking part in another clinical trial involving a medicinal product
- People who have a condition that would make the blood collection procedures required by the trial unsafe or not possible
- People whose psychological, family, geographical, or social circumstances, in the opinion of the trial investigator, could affect their ability to sign a consent form or follow the trial procedures
- People who are under a legal protection arrangement such as curatorship, guardianship, or judicial protection
- People who are pregnant or currently breastfeeding
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
Phone: +33478782666
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
Best pharmacokinetic (PK) indicator of response to treatment in patients with AML - Biological endpoint; Best pharmacokinetic (PK) indicator of response to treatment in patients with AML - Biological endpoint; Best pharmacokinetic (PK) indicator of response to treatment in patients with AML - Biological endpoint; Best pharmacokinetic (PK) indicator of response to treatment in patients with AML - Biological endpoint; Best pharmacokinetic (PK) indicator of response to treatment in patients with AML - Clinical Endpoint
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.