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:
- Adults aged 18 and older who have been newly diagnosed with a type of blood cancer called Ph- B-ALL or T-ALL (specific forms of acute lymphoblastic leukaemia)
- People whose treating doctor considers them unsuitable for a standard intensive chemotherapy approach (sometimes called a "pediatric-inspired regimen"), for reasons such as older age (around 40 or above) or concerns about tolerating that type of treatment
- People whose leukaemia is detectable in the bone marrow or blood through a specialised laboratory test called multi-parameter flow cytometry
- People who are reasonably well and able to carry out basic daily activities (this is measured on a standard medical scale; a lower level of functioning may be accepted if leukaemia is directly causing it)
- People whose liver function test results fall within acceptable ranges as defined by the trial (confirm with trial site for specific values)
- People whose kidneys are working at an adequate level, as measured by a specific calculation (confirm with trial site)
- People who are expected to survive at least 3 months from causes unrelated to their leukaemia
- People who are able to understand the study information and agree to take part
- Women who could become pregnant must use effective non-hormonal contraception during treatment and for 3 months after the last dose; men with partners who could become pregnant must use effective contraception from signing the consent form until at least 3 months after the last dose
Who may not be able to join:
- People who have already received systemic treatment for ALL, beyond very limited amounts of specific medications used to manage urgent symptoms (confirm with trial site for what is permitted)
- People diagnosed with a related but different condition called Burkitt lymphoma or Burkitt leukaemia
- People whose leukaemia is only present outside the bone marrow, or who have known leukaemia involvement in the brain or spinal fluid
- People with a known allergy or intolerance to any of the study drugs
- People with a history of severe pancreatitis (grade 3 or higher) or a long-term condition affecting pancreas function
- People with known active chronic liver disease, such as cirrhosis, non-alcoholic fatty liver disease, or a related condition
- People with other medical or mental health conditions that the treating doctor believes would make participation unsafe
- People who are pregnant or breastfeeding (a pregnancy test may be required for some women before joining)
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: Ryan D. Cassaday, MD, Fred Hutch/University of Washington Cancer Consortium
Phone: 206-606-8311
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
Measurable residual disease (MRD) negativity
Can't join this trial?
Data last synced from ClinicalTrials.gov: 15 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.