NotablePrimary and study completion pushed from Oct 15, 2026 to Apr 15, 2027Show 4 more changesShow less
Enrollment increased: 137 → 193 participants
Eligibility criteria expanded, about 10 words
Secondary endpoints: details revised at 7 of 15 entries
Site details revised at 2 of 61 sites
MinorTrial status: Recruiting to Active, Not Recruiting
Enrollment target: estimated 200 to confirmed 137
Study sites: 62 to 61
v33
Minor2 versionsRe-verified since Jul 25, 2025, no change to tracked fieldsv31-v32
MinorSite details revised at 1 of 62 sitesv30
MinorSite details revised at 7 of 62 sitesv29
Show 27 earlier versionsHide 27 earlier versions
MinorSite details revised at 7 of 62 sitesv28
MinorStudy sites: 61 to 62v27
MinorSite details revised at 3 of 61 sitesv26
MinorStudy sites: 55 to 61v25
MinorSite details revised at 8 of 55 sitesv24
NotablePrimary and study completion dates: Apr 15, 2026 to Oct 15, 2026v23
MinorStudy sites: 54 to 55v22
Minor2 versionsRe-verified since Jul 18, 2024, no change to tracked fieldsv20-v21
MinorStudy sites: 53 to 54v19
MinorStudy sites: 51 to 53v18
MinorStudy sites: 50 to 51v17
MinorStudy sites: 46 to 50v16
MinorStudy sites: 38 to 46v15
MinorStudy sites: 36 to 38v14
MinorRe-verified, no change to tracked fieldsv13
MinorStudy sites: 35 to 36v12
MinorStudy sites: 31 to 35v11
MinorSite details revised at 29 of 31 sitesv10
MinorStudy sites: 28 to 31v9
MinorStudy sites: 16 to 28v8
MinorStudy sites: 8 to 16v7
MinorRe-verified, no change to tracked fieldsv6
MinorStudy sites: 5 to 8v5
MinorStudy sites: 2 to 5v4
MinorStudy sites: 1 to 2v3
NotableTrial status: Not Yet Recruiting to Recruiting
Study sites: 0 to 1
Start date changed from estimate of Dec 15, 2022 to Dec 12, 2022
v2
MinorStudy First Submitted
Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Retention rate of acalabrutinib in a non-interventional setting. This is a prospective, multicentre, non-interventional study to collect real-world data on retention rates of CLL patients prescribed with acalabrutinib in Germany.