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 been diagnosed with chronic lymphocytic leukaemia (CLL), a type of blood cancer, and have not yet received any treatment for it
- People who were started on a medication called acalabrutinib through the UK Early Access Programme (a scheme that allowed patients to receive the drug before it was widely available)
- People who received their first dose of acalabrutinib between 1 April 2020 and 1 April 2021
- People who were 18 years of age or older at the time of treatment
- People later found to have a closely related condition called small lymphocytic lymphoma (SLL) may also be eligible (confirm with trial site)
Who may not be able to join:
- No exclusion criteria are listed in the study protocol
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: Toby A Eyre, Department of Clinical Haematology, Oxford University Hospitals NHS Foundation Trust, Oxford, UK
Phone: 1-877-240-9479
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
Real-world progression free survival (rwPFS); Real-world progression free survival (rwPFS); Real-world progression free survival (rwPFS); Real-world progression free survival (rwPFS); Real-world progression free survival (rwPFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.