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Observational Study of Acalabrutinib in Patients With Chronic Lymphocytic Leukaemia in the United Kingdom

Study acronym: EPIC
StatusRecruiting
PhaseNot specified
Started2022-10-17
View on ClinicalTrials.gov ↗
This is a retrospective observational research study to describe the characteristics and real-world clinical outcomes of patients with chronic lymphocytic leukaemia receiving acalabrutinib in the United Kingdom (the EPIC study). Physicians treating chronic lymphocytic leukaemia patients with acalabrutinib, where the patients started treatment as part of the acalabrutinib Early Access Programme (EAP), will be invited to recruit patients. Clinical data will be extracted from the patients' clinical records in line with local laws. Data from this study will provide UK-specific real-world data on patients who were started on acalabrutinib as part of the UK acalabrutinib EAP.

Amendment history 1 change detected by DataLookout

2026-09-10
notable
Enrollment reduced: 350 → 287 participants
Trial Details
NCT Number NCT05557695
Lead Sponsor AstraZeneca
Collaborators: UKCLL Forum
Conditions Chronic Lymphocytic Leukemia, CLL
Enrollment 287 participants
Start Date 2022-10-17
Primary Completion 2027-04-01 (estimated)
Study Completion 2027-04-01 (estimated)
Updated on ClinicalTrials.gov 2026-09-09