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Recruiting Phase 3 Interventional

A Study of Nemtabrutinib Plus Venetoclax vs Venetoclax + Rituximab (VR) in Second-line (2L) + Relapsed/Refractory (R/R) Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma (CLL/SLL) (MK-1026-010/BELLWAVE-010).

ClinicalTrials.gov ID: NCT05947851

Public ClinicalTrials.gov record NCT05947851. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 21, 2026, 6:59 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3, Open-label, Randomized Study to Compare the Efficacy and Safety of Nemtabrutinib (MK-1026) Plus Venetoclax Versus Venetoclax Plus Rituximab in Participants With Relapsed/Refractory Chronic Lymphocytic Leukemia/Small Lymphocytic Lymphoma Following at Least 1 Prior Therapy (BELLWAVE-010)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to assess the safety and tolerability and to confirm the dose of nemtabrutinib in combination with venetoclax in participants with R/R CLL/SLL. The primary study hypotheses are that the combination of nemtabrutinib plus venetoclax is superior to VR with respect to progression-free survival (PFS) per 2018 International Workshop on Chronic Lymphocytic Leukemia (iwCLL) criteria as assessed by blinded independent central review (BICR).

Study identification

NCT ID
NCT05947851
Recruitment status
Recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
Merck Sharp & Dohme LLC
Industry
Enrollment
735 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 8, 2023 (Actual)
Primary completion
Jun 1, 2032 (Estimated)
Completion
Jul 1, 2035 (Estimated)
Last update posted
Oct 15, 2026

2023 – 2035

United States locations

U.S. sites
25
U.S. states
19
U.S. cities
25
Facility City State ZIP Site status
Highlands Oncology Group ( Site 5405) Springdale Arkansas 72762 Recruiting
MemorialCare Health System - Long Beach Medical Center ( Site 5421) Long Beach California 90806 Recruiting
Clermont Oncology Center ( Site 5430) Clermont Florida 34711 Recruiting
Memorial Hospital West ( Site 5410) Pembroke Pines Florida 33028 Recruiting
Fort Wayne Medical Oncology and Hematology ( Site 5444) Fort Wayne Indiana 46804 Recruiting
Center for Cancer and Blood Disorders ( Site 5439) Bethesda Maryland 20817 Recruiting
Avera Cancer Institute - Marshall ( Site 5462) Marshall Minnesota 56258 Recruiting
Hattiesburg Clinic Hematology/Oncology ( Site 5416) Hattiesburg Mississippi 39401 Recruiting
MidAmerica Cancer Care, LLC ( Site 5426) Kansas City Missouri 64132 Recruiting
Intermountain Health St. Vincent Regional Hospital - Cancer Centers of Montana ( Site 5433) Billings Montana 59102 Recruiting
Renown Regional Medical Center-Renown Health Medical Oncology ( Site 5434) Reno Nevada 89502 Recruiting
Atlantic Health System Morristown Medical Center ( Site 5445) Morristown New Jersey 07960 Recruiting
New York Oncology Hematology, P.C. ( Site 5453) Albany New York 12208 Recruiting
Oregon Health and Science University ( Site 5425) Portland Oregon 97239-3011 Recruiting
Avera Cancer Institute - Aberdeen ( Site 5458) Aberdeen South Dakota 57401 Recruiting
Avera Cancer Institute - Mitchell ( Site 5461) Mitchell South Dakota 57301 Recruiting
Avera Cancer Institute - Pierre ( Site 5460) Pierre South Dakota 57501 Recruiting
Avera Cancer Institute- Research ( Site 5437) Sioux Falls South Dakota 57105 Recruiting
Avera Cancer Institute - Yankton ( Site 5459) Yankton South Dakota 57078 Recruiting
PatientCare Clinical Research LLC ( Site 5435) Sugar Land Texas 77479 Recruiting
University of Virginia Cancer Center ( Site 5402) Charlottesville Virginia 22903 Recruiting
Vista Oncology ( Site 5449) Olympia Washington 98506 Recruiting
Medical Oncology Associates, PS ( Site 5406) Spokane Washington 99208 Recruiting
West Virginia University ( Site 5447) Morgantown West Virginia 26506 Recruiting
University of Wisconsin Hospital and Clinics-Carbone Cancer Center ( Site 5423) Madison Wisconsin 53792 Completed

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 74 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05947851, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 15, 2026 · Synced Oct 21, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05947851 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →