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Taking people in BelarusNo phase

Observes acalabrutinib use in adults with chronic lymphocytic leukemia in Belarus

Studies how acalabrutinib is used in adults with chronic lymphocytic leukemia in routine care.

Plain-language title generated from the registry record
Registry title: Observ Prosp Study of Acalabrutinib in CLL Therapy in Real Clinical Practice in Belarus

Key facts

Where
Grodno, Homyel, Minsk, and Mogilev, BelarusSee the 4 sites

Where in Belarus

  • GrodnoGrodno, BelarusTaking people
  • HomyelHomyel, BelarusNot yet recruiting
  • MinskMinsk, BelarusTaking people
  • MogilevMogilev, BelarusTaking people

Questions to ask the study team

  1. How often do I need to come in, and for how long each time?
  2. Are travel costs paid?
  3. Can I keep my own doctor?
  4. What happens if I want to stop?
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Trial details

Who runs it
AstraZeneca
Trial code
NCT07288515
Record updated
9 September 2026
Original description
to address critical gap in knowledge, providing essential data on the real-world effectiveness, safety, associated with acalabrutinib treatment in patients with CLLRead full original descriptionShow less

Observational Prospective Study of Acalabrutinib in Chronic Lymphocytic Leukemia Therapy in Real Clinical Practice in Belarus.

to address critical gap in knowledge, providing essential data on the real-world effectiveness, safety, associated with acalabrutinib treatment in patients with CLL

Inclusion: Age ≥18 years; Confirmed diagnosis of CLL; Newly prescribed acalabrutinib monotherapy within the previous four weeks preceding study enrolment. Monotherapy is defined as acalabrutinib prescribes without concomitant administration (or planned initiation) of other anti-leukemic agents (e.g. obinutuzumab, venetoclax, bendamustine) within ± 30 days of acalabrutinib initiation; Treatment-naïve or R/R CLL; Ability and willingness to provide informed consent for study participation.

Exclusion: Prior treatment with any BTK inhibitor; Patients not satisfying any of the inclusion criteria; Participation in other ongoing clinical trials; Pregnant or breastfeeding females.

ClinicalTrials.gov NCT07288515