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 given written consent to participate (or whose legal representative has done so on their behalf)
- People who agree to allow stored tumour tissue samples from their diagnosis to be used in the study
- People aged 18 or older
- People whose general physical functioning meets a certain level of activity (known as ECOG score of 3 or below — confirm with trial site)
- People who have been diagnosed with a specific type of blood cancer called Acute Myeloid Leukaemia (AML), confirmed through laboratory testing
- People whose AML has come back or has not responded to previous treatment — specifically, at least one prior treatment for those with higher-risk disease, or at least two prior treatments for those with lower- or moderate-risk disease
- People who have enough cancer cells available in their bone marrow or blood for specialised laboratory testing (either through a blood sample with enough circulating cancer cells, a bone marrow sample with enough cancer cells present, bone marrow biopsy fluid if a standard sample cannot be obtained, or a sample from disease outside the bone marrow if accessible)
- People whose life expectancy is expected to be greater than 100 days
- People who have recovered from most side effects of previous cancer treatment (minor ongoing side effects at a low level, and hair loss, are acceptable)
Who may not be able to join:
- People who have a specific chromosomal change called t(15;17), or a subtype of AML known as acute promyelocytic leukaemia (APL or FAB M3)
- People with active cancer in the central nervous system (brain or spinal cord) that has not been treated or is not responding to treatment
- People with active graft versus host disease (a complication that can occur after a bone marrow or stem cell transplant)
- People with unstable heart conditions, including a heart attack within the past 6 months, uncontrolled irregular heart rhythm (atrial fibrillation), or uncontrolled high blood pressure
- People with a serious uncontrolled illness
- People with an uncontrolled active infection
- People who are pregnant or breastfeeding
- People with another serious condition or active cancer that the trial doctor believes would make participation unsafe
- People who, in the trial doctor's judgement, may have difficulty following all study procedures for any reason
- People who are planning to receive a live vaccine during the study period
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: Pamela Becker, MD, City of Hope Medical Center
Phone: 626-218-2405
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
Feasibility - Obtaining HopeSeq and CDST
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.