Observ prosp study of acalabrutinib in CLL therapy in real clinical practice in Belarus - ALICIA(BY)

Study identifier:D8220R00090

ClinicalTrials.gov identifier:NCT07288515

EudraCT identifier:N/A

CTIS identifier:N/A

Will Be Recruiting

Official Title

Observational prospective study of acalabrutinib in chronic lymphocytic leukemia therapy in real clinical practice in Belarus.

Medical condition

Chronic Lymphocytic Leukemia

Phase

N/A

Healthy volunteers

No

Study drug

-

Sex

All

Estimated Enrollment

50

Study type

Observational

Age

18 Years - n/a

Date

Study Start Date: 31 Dec 2025
Estimated Primary Completion Date: 31 Dec 2029
Estimated Study Completion Date: 31 Dec 2029

Study design

Allocation: N/A
Endpoint Classification: -
Intervention Model: -
Masking: -
Primary Purpose: -

Verification:

Verified 01 Nov 2025 by AstraZeneca

Sponsors

AstraZeneca

Collaborators

-

Inclusion and exclusion criteria