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Clinical Trials in China / NCT05624554
Active, not recruiting Phase 3

A Study of Nemtabrutinib vs Chemoimmunotherapy for Participants With Previously Untreated Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL) Without TP53 Aberrations (MK-1026-008, BELLWAVE-008)

NCT05624554 · tracked via the Priya Life Science China tracker
Sponsor
Merck Sharp & Dohme LLC
Phase
Phase 3
Started
2023-03-16
Last updated
2026-03-16

Condition(s) studied

Chronic Lymphocytic LeukemiaSmall Lymphocytic Lymphoma

Investigational drug(s) / intervention(s)

NemtabrutinibFludarabineCyclophosphamideBendamustineRituximabTruximaRuxienceRiabni

Nemtabrutinib: 65 mg administered orally daily until disease progression, unacceptable toxicity, or discontinuation criteria met.

Fludarabine: 25 mg/m\^2 administered via intravenous (IV) infusion on Days 1, 2, and 3 of each 28-day cycle up to 6 cycles.

Cyclophosphamide: 250 mg/m\^2 administered via IV infusion on Days 1, 2, and 3 of each 28-day cycle up to 6 cycles.

Bendamustine: Administered via IV infusion on Days 1 and 2 of each 28-day cycle up to 6 cycles. The first dose is given as 70 to 90 mg/m\^2. Subsequent doses may be escalated up to 90 mg/m\^2, if applicable and as per local guidelines.

Rituximab: Administered as an IV infusion on Day 1 of each 28-day cycle. The initial dose is 375 mg/m\^2 (cycle 1) followed by 500 mg/m\^2 for remaining cycles.

Truxima: Administered as an IV infusion on Day 1 of each 28-day cycle. The initial dose is 375 mg/m\^2 (cycle 1) followed by 500 mg/m\^2 for remaining cycles.

Ruxience: Administered as an IV infusion on Day 1 of each 28-day cycle. The initial dose is 375 mg/m\^2 (cycle 1) followed by 500 mg/m\^2 for remaining cycles.

Riabni: Administered as an IV infusion on Day 1 of each 28-day cycle. The initial dose is 375 mg/m\^2 (cycle 1) followed by 500 mg/m\^2 for remaining cycles.

Study summary

Researchers are looking for new ways to treat people with chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL). CLL and SLL are types of blood cancer. Researchers want to know if people who take nemtabrutinib compared to those who take the standard treatments in this study will live longer without their cancer growing, spreading or returning (progression free survival).

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
The main inclusion and exclusion criteria include but are not limited to the following: Inclusion Criteria: * Confirmed diagnosis of chronic lymphocytic leukemia (CLL)/ small lymphocytic lymphoma (SLL) and active disease clearly documented to have a need to initiate therapy * Has previously untreated CLL/SLL participants without tumor protein 53 (TP53) aberrations and documented 11q status and immunoglobulin heavy chain gene (IGHV) mutational status * The ability to swallow and retain oral medication Exclusion Criteria: * Has active hepatitis B virus (HBV) or hepatitis C virus (HCV) infection * Has gastrointestinal dysfunction that may affect drug absorption (eg, gastric bypass surgery, gastrectomy) * Has known additional malignancy that is progressing or has required active treatment within the past 3 years, except basal cell carcinoma of skin, squamous cell carcinoma of skin, or carcinoma in situ (eg, breast carcinoma, cervical cancer in situ) that have undergone potential curative therapy * Has history of severe bleeding disorders * Has not adequately recovered from major surgery or has ongoing surgical complications

Primary outcome measure(s)

Trial sites (97)

FacilityCityRegionStatus
Highlands Oncology Group ( Site 5205) Springdale Arkansas
Clermont Oncology Center ( Site 5224) Clermont Florida
Hattiesburg Clinic Hematology/Oncology ( Site 5216) Hattiesburg Mississippi
Medical Oncology Associates, PS ( Site 5206) Spokane Washington
Royal Adelaide Hospital ( Site 1105) Adelaide South Australia
Hospital Erasto Gaertner-CEPEP - Pesquisa Clínica ( Site 1317) Curitiba Paraná
Hospital Amaral Carvalho-Centro de Pesquisas ( Site 1304) Jaú São Paulo
A. C. Camargo Cancer Center ( Site 1318) São Paulo São Paulo
Instituto Nacional de Câncer - INCA-Divisão de Pesquisa Clínica e Desenvolvimento Tecnológico HC1 ( Site 1319) Rio de Janeiro Brazil
ICESP - INSTITUTO DO CÂNCER DO ESTADO DE SÃO PAULO-Pesquisa Clinica ( Site 1308) São Paulo Brazil
Hospital Paulistano-Americas Oncologia ( Site 1302) São Paulo Brazil
Specialized Hospital for Active Treatment of Haematology Diseases ( Site 6403) Sofia Sofia (stolitsa)
University Multiprofile Hospital for Active Treatment "Sveti Georgi" EAD ( Site 6404) Plovdiv Bulgaria
Medical Centre Pratia Clinic EOOD ( Site 6406) Plovdiv Bulgaria
UMHAT "Prof. Dr. Stoyan Kirkovich"AD-Clinical Hematology ( Site 6400) Stara Zagora Bulgaria
Multriprofile Hospital for Active Treatment "Hristo Botev" ( Site 6402) Vratsa Bulgaria
James Lind Centro de Investigacion del Cancer ( Site 1503) Temuco Araucania
Biocenter ( Site 1507) Concepción Biobio
IC La Serena Research ( Site 1506) La Serena Coquimbo Region
Centro de Estudios Clínicos SAGA-CECSAGA ( Site 1509) Santiago Region M. de Santiago
FALP-UIDO ( Site 1500) Santiago Region M. de Santiago
Clínica Inmunocel ( Site 1511) Santiago Region M. de Santiago
Peking University Third Hospital ( Site 1602) Beijing Beijing Municipality
Chongqing University Cancer Hospital ( Site 1605) Chongqing Chongqing Municipality
Chongqing University Three Gorges Hospital ( Site 1609) Chongqing Chongqing Municipality
Southern Medical University Nanfang Hospital-Department of Hematopathology ( Site 1607) Guangzhou Guangdong
Sun Yat-sen University Cancer Center ( Site 1608) Guangzhou Guangdong
The Affiliated Hospital of Guizhou Medical University ( Site 1625) Guiyang Guizhou
Hainan General Hospital ( Site 1603) Haikou Hainan
Henan Cancer Hospital-hematology department ( Site 1613) Zhengzhou Henan
Tongji Hospital Tongji Medical,Science & Technology ( Site 1619) Wuhan Hubei
Union Hospital Tongji Medical College Huazhong University of Science and Technology ( Site 1618) Wuhan Hubei
Xiangya Hospital Central South University-Hematology department ( Site 1616) Changsha Hunan
Hunan Cancer Hospital ( Site 1615) Changsha Hunan
The First Affiliated Hospital of Soochow University-hematology department ( Site 1612) Suzhou Jiangsu
The First Affiliated Hospital of Nanchang University ( Site 1614) Nanchang Jiangxi
Jiangxi Provincial Cancer Hospital ( Site 1628) Nanchang Jiangxi
The First Hospital of Jilin University-Hematology ( Site 1621) Changchun Jilin
The First Affiliated Hospital of Xi'an Jiaotong University ( Site 1617) Xi'an Shaanxi
Shaanxi provincial people's hospital ( Site 1626) Xi'an Shaanxi

+ 57 more sites — see the full list on the official registry below.

On this site

📄 Rituxan (rituximab) drug profile →

More Merck Sharp & Dohme LLC trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05624554 on ClinicalTrials.gov ↗ ← All trials in China