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NCT05645172Active, not recruiting

Retention Rate of Acalabrutinib in a Non-interventional Setting

Source: ClinicalTrials.gov · Last updated 16 Oct 2026

Brief summary (registry, in English)

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.

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
193 (actual)
First submitted
10 Nov 2022
Start date
12 Dec 2022
Primary completion date
15 Apr 2027
Lead sponsor
AstraZeneca
NCT number
NCT05645172

What you commit to

  • Study type: Observational
  • Participants enrolled: 193
  • From 12 Dec 2022 to the primary completion date, 15 Apr 2027
  • 54 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Contraindications to treatment with acalabrutinib according to the current SmPC
  • Disease progression on prior BTKi therapy
  • Start of acalabrutinib therapy more than 28 days prior to enrolment

Other

  • Current or planned participation in an interventional clinical trial
  • Pregnancy or breast feeding

Who the study is looking for

  • Age ≥ 18 years
  • Diagnosis of CLL
  • Ability to understand the study concept and to regularly complete patient questionnaires from physical, mental, and linguistic perspectives
  • Decision to start therapy with acalabrutinib according to the current SmPC. For previously untreated patients as continuous therapy with or without obinutuzumab. OR For patients with at least one prior CLL therapy as continuous monotherapy.
  • Provision of signed informed consent form

Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (54)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
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AmbergGermanyUnknown status
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AschaffenburgGermanyUnknown status
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AugsburgGermanyUnknown status
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Bad HomburgGermanyUnknown status
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Bad LiebenwerdaGermanyUnknown status
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BautzenGermanyUnknown status
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BerlinGermanyUnknown status
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BonnGermanyUnknown status
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DachauGermanyUnknown status
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DelitzschGermanyUnknown status
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DessauGermanyUnknown status
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DortmundGermanyUnknown status
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D RenGermanyUnknown status
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ErfurtGermanyUnknown status
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EssenGermanyUnknown status
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Frankfurt am MainGermanyUnknown status
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GarbsenGermanyUnknown status
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HalleGermanyUnknown status
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HanoverGermanyUnknown status
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HeideGermanyUnknown status
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Herrsching am AmmerseeGermanyUnknown status
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HertenGermanyUnknown status
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HofGermanyUnknown status
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KulmbachGermanyUnknown status
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LaatzenGermanyUnknown status
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LandshutGermanyUnknown status
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LebachGermanyUnknown status
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LeipzigGermanyUnknown status
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L RrachGermanyUnknown status
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M NchenGermanyUnknown status
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MoersGermanyUnknown status
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NaunhofGermanyUnknown status
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Neustadt Am R BenbergeGermanyUnknown status
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N RnbergGermanyUnknown status
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OldenburgGermanyUnknown status
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PaderbornGermanyUnknown status
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PasingGermanyUnknown status
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PirnaGermanyUnknown status
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Porta WestfalicaGermanyUnknown status
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PotsdamGermanyUnknown status
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RemscheidGermanyUnknown status
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ReutlingenGermanyUnknown status
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RiesaGermanyUnknown status
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SaalfeldGermanyUnknown status
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Saarbr CkenGermanyUnknown status
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SchkeuditzGermanyUnknown status
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SchorndorfGermanyUnknown status
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SiegburgGermanyUnknown status
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SindelfindenGermanyUnknown status
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StraubingGermanyUnknown status
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TwistringenGermanyUnknown status
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WeidenGermanyUnknown status
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W RselenGermanyUnknown status
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ZittauGermanyUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.