Study identifier:D822BC00001
ClinicalTrials.gov identifier:NCT04075292
EudraCT identifier:N/A
CTIS identifier:N/A
A Randomized, Multicenter, Open-Label, Phase 3 Study to Evaluate the Efficacy and Safety of Acalabrutinib versus Chlorambucil plus Rituximab in Subjects with Previously Untreated Chronic Lymphocytic Leukemia
Untreated Chronic Lymphocytic Leukemia
Phase 3
No
Acalabrutinib, Rituximab, Chlorambucil
All
155
Interventional
18 Years - 130 Years
Allocation: Randomized
Endpoint Classification: -
Intervention Model: Parallel Assignment
Masking: -
Primary Purpose: Treatment
Verified 01 Apr 2025 by AstraZeneca
AstraZeneca
-
This is a randomized, multicenter, open-label, Phase 3 study to evaluate the efficacy and safety of Acalabrutinib versus Chlorambucil plus Rituximab in subjects with Previously Untreated Chronic Lymphocytic Leukemia.
Patients be randomized in a 1:1 ratio into 2 arms to receive either acalabrutinib monotherapy (Arm A) or rituximab in combination with chlorambucil (Arm B). The primary objective of this study is to compare the efficacy of acalabrutinib relative to chlorambucil plus rituximab in subjects with previously untreated chronic lymphocytic leukemia without del(17p) or TP53 mutation.
Location
Location
Bangkok, Thailand, 10330
Location
Bangkok, Thailand, 10700
Location
Chiang Mai, Thailand, 50200
Location
Khon Kaen, Thailand, 40002
Location
Bangkok, Thailand, 10400
Location
Kaohsiung, Taiwan, Province of China, 833
Location
Tainan, Taiwan, Province of China, 704
Location
Taipei, Taiwan, Province of China, 11217
Arms | Assigned Interventions |
---|---|
Experimental: Acalabrutinib Acalabrutinib will be orally administered until disease progression or unacceptable toxicity | Drug: Acalabrutinib acalabrutinib 100 mg twice daily orally |
Active Comparator: Rituximab and Chlorambucil Chlorambucil orally administered and Rituximab via IV infusion for 6 cycles | Drug: Rituximab Rituximab: 375 mg/m2 IV infusion on Day 1 of Cycle 1. 500 mg/m2 IV infusion on Day 1 for each of subsequent cycles (Cycles 2-6) Drug: Chlorambucil Chlorambucil: 0.5 mg/kg body weight orally on Day 1 and Day 15 of Cycles 1-6 |
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