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 fully understand the study, choose to take part voluntarily, and sign a consent form
- People aged between 18 and 65 years old
- People who have been diagnosed with acute myeloid leukemia (a type of blood cancer, but not a specific subtype called APL) that has not yet been treated, and who also meet at least one of the following: their leukemia developed from a prior blood condition (secondary AML); their leukemia developed as a result of previous cancer treatment (therapy-related AML); their leukemia has spread outside the bone marrow to form a tumour (myeloid sarcoma); or they are aged 60 or older and have been assessed by doctors as healthy enough to receive intensive treatment
- People whose heart is working well, with the heart's pumping strength (called ejection fraction) at 50% or above
- People whose liver and kidney blood test results fall within acceptable ranges as determined by the trial team
- People whose general health and ability to carry out daily activities is rated at a level of 0, 1, or 2 on a standard medical scale (where 0 means fully active and 2 means able to care for oneself but unable to do physical work)
Who may not be able to join:
- People whose leukemia has been assessed by doctors as making them too unwell or too frail to tolerate intensive treatment
- People who have, or have had, another type of cancer that currently requires treatment
- People with serious uncontrolled health conditions, such as a severe active infection or high blood pressure that cannot be managed
- People who have had a significant allergic reaction to medications in the same family as the drugs used in this trial
- People who are pregnant or breastfeeding, or people who are unwilling to use reliable contraception throughout the study period
- People with a history of serious neurological or psychiatric conditions
- People with serious heart conditions, such as a previous heart attack, severe chest pain, or serious heart rhythm problems
- People who have had a stroke or a temporary stroke-like episode (confirm with trial site)
- People with a known HIV infection, or an active hepatitis B or C infection (note: people who are inactive carriers of hepatitis, or who have low virus levels while receiving certain antiviral treatments, may not be automatically excluded — confirm with trial site)
- People who have taken certain medications or consumed certain foods that affect how the body processes drugs (specifically, strong or moderate CYP3A inducers or inhibitors, or strong P-gp inhibitors) within the 7 days before starting the trial treatment
- People who are unable to swallow tablets or capsules, or who have a condition that prevents the body from properly absorbing oral medications
- People whom the trial doctors determine are not suitable for the study 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.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Composite Complete Remission Rate
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.