RecruitingNCT07288515

Observ Prosp Study of Acalabrutinib in CLL Therapy in Real Clinical Practice in Belarus

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


Sponsor

AstraZeneca

Enrollment

50 participants

Start Date

Dec 31, 2025

Study Type

OBSERVATIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 Years

Inclusion Criteria8

  • 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.
  • Prior treatment with any BTK inhibitor.
  • Participation in other ongoing clinical trials.
  • Pregnant or breastfeeding females

Locations(1)

Research Site

Minsk, Belarus

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT07288515


Related Trials