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 already enrolled in a database called PLATON
- People who are 18 years of age or older
- People who have been diagnosed with a type of blood cancer called CLL and have not previously received any treatment for it, but are currently being treated with a medicine called acalabrutinib (either on its own or combined with another medicine called obinutuzumab) in a standard clinical setting
- People who are comfortable with their health information, already collected as part of the PLATON study, being used for research purposes
- People who started treatment with acalabrutinib but stopped taking it before 12 months have passed
Who may not be able to join:
- People who are pregnant
- People who are under legal protection or guardianship arrangements (confirm with trial site)
- People who are 18 or older but are unable to communicate whether they object to their data being used
- People who have previously received other treatments for CLL before this study
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: 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
To measure QoL score of CLL patients treated with acalabrutinib, from treatment initiation and up to 12 months
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.