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Taking people in ChinaPhase 3

Sonrotoclax plus zanubrutinib versus venetoclax plus acalabrutinib in untreated chronic lymphocytic leukemia

Compares two drug pairs in adults with chronic lymphocytic leukemia not yet treated.

Plain-language title generated from the registry record
Registry title: A Study to Investigate Sonrotoclax (BGB-11417) Plus Zanubrutinib (BGB-3111) Compared With Venetoclax Plus Acalabrutinib in Adults With Previously Untreated Chronic Lymphocytic Leukemia

Key facts

Where
Beijing, Changsha, Chengdu, Chongqing, Fuzhou, Guangzhou, Guiyang, Hangzhou, Harbin, Jinan, Kunming, Nanchang, Nanjing, Nanning, Nantong, Shanghai, Tianjin, Xi'an, and Zhengzhou, ChinaSee the 20 sites
Phase
Phase 3

Where in China

  • Peking Union Medical College HospitalBeijing, ChinaTaking people
  • The Second Xiangya Hospital of Central South UniversityChangsha, ChinaTaking people
  • Sichuan Academy of Medical Sciences and Sichuan Provincial Peoples HospitalChengdu, ChinaTaking people
  • The First Affiliated Hospital of Chongqing Medical UniversityChongqing, ChinaTaking people
  • The First Affiliated Hospital of Fujian Medical UniversityFuzhou, ChinaTaking people
  • Sun Yat Sen University Cancer Center Huangpu BranchGuangzhou, ChinaTaking people
  • Zhujiang Hospital of Southern Medical UniversityGuangzhou, ChinaNo longer taking part
  • Guizhou Provincial Peoples HospitalGuiyang, ChinaTaking people
  • The First Affiliated Hospital, Zhejiang University School of MedicinechengzhanHangzhou, ChinaTaking people
  • Harbin Medical University Cancer HospitalHarbin, ChinaTaking people
  • Shandong Provincial HospitalJinan, ChinaTaking people
  • First Affiliated Hospital of Kunming Medical UniversityKunming, ChinaTaking people
  • The Second Affiliated Hospital of Nanchang UniversityNanchang, ChinaTaking people
  • Jiangsu Province HospitalNanjing, ChinaTaking people
  • The First Affiliated Hospital of Guangxi Medical UniversityNanning, ChinaTaking people
  • Affiliated Hospital of Nantong UniversityNantong, ChinaTaking people
  • Rui Jin Hospital Shanghai Jiao Tong University School of MedicineShanghai, ChinaTaking people
  • Institute of Hematology and Hospital of Blood DiseaseTianjin, ChinaTaking people
  • The Second Affiliated Hospital of XiAn Jiaotong UniversityXi'an, ChinaTaking people
  • Henan Cancer HospitalZhengzhou, ChinaTaking people

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  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
BeOne Medicines
Trial code
NCT07277231EU 2025-524366-21-00
Record updated
28 September 2026
Original description
The purpose of this study is to investigate the efficacy and safety of fixed-duration sonrotoclax (also known as BGB-11417) plus zanubrutinib (also known as BGB-3111) (SZ) compared with fixed-duration of venetoclax plus acalabrutinib (AV) in participants with previously untreated chronic lymphocytic leukemia (CLL).Read full original descriptionShow less

A Phase 3, Open-Label, Randomized Study of Sonrotoclax (BGB-11417) Plus Zanubrutinib (BGB-3111) Compared With Venetoclax Plus Acalabrutinib in Patients With Previously Untreated Chronic Lymphocytic Leukemia

The purpose of this study is to investigate the efficacy and safety of fixed-duration sonrotoclax (also known as BGB-11417) plus zanubrutinib (also known as BGB-3111) (SZ) compared with fixed-duration of venetoclax plus acalabrutinib (AV) in participants with previously untreated chronic lymphocytic leukemia (CLL).

Inclusion: Treatment-naïve (TN) adults with confirmed diagnosis of CLL which requires treatment; Eastern Cooperative Oncology Group (ECOG) score 0, 1, or 2; Measurable disease by Computer Tomography/Magnetic Resonance Imaging; Adequate bone marrow and organ function.

Exclusion: Previous systemic treatment for CLL; Known prolymphocytic leukemia or history of, or currently suspected, Richter's transformation; History of confirmed progressive multifocal leukoencephalopathy (PML); Uncontrolled hypertension or clinically significant cardiovascular disease; Note: Other protocol defined Inclusion/Exclusion criteria may apply; Known central nervous system involvement.

ClinicalTrials.gov NCT07277231 · EU CTIS 2025-524366-21-00