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Active, not recruiting Phase 2 Interventional

A Study to Investigate Sonrotoclax Combined With Zanubrutinib Versus Zanubrutinib Alone in Participants With Previously Untreated Chronic Lymphocytic Leukemia

ClinicalTrials.gov ID: NCT06637501

Public ClinicalTrials.gov record NCT06637501. 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 Nov 1, 2026, 8:48 AM EST

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

Official title

A Multicenter, Open-Label, Phase 2 Study to Investigate the Efficacy and Safety of Sonrotoclax Combined With Zanubrutinib Compared With Zanubrutinib Monotherapy in Adult Patients With Previously Untreated Chronic Lymphocytic Leukemia

Brief summary

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

The purpose of this study is to support the registration plan of sonrotoclax plus zanubrutinib treatment in participants with previously untreated chronic lymphocytic leukemia (CLL). This study is designed to assess the contribution of sonrotoclax to the efficacy outcome of the combination of zanubrutinib and sonrotoclax.

Study identification

NCT ID
NCT06637501
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 2
Lead sponsor
BeOne Medicines
Industry
Enrollment
94 participants

Conditions and interventions

Interventions

Drug

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
Nov 14, 2024 (Actual)
Primary completion
Nov 2026 (Estimated)
Completion
Sep 2029 (Estimated)
Last update posted
Jul 9, 2026

2024 – 2029

United States locations

U.S. sites
11
U.S. states
8
U.S. cities
9
Facility City State ZIP Site status
Cleveland Clinic Florida Weston Florida 33331-3609 —
Northwest Georgia Oncology Centers Marietta Marietta Georgia 30060-1152 —
Illinois Cancer Specialists (Niles) Usor Niles Illinois 60714-5905 —
The University of Maryland Greenebaum Comprehensive Cancer Center Baltimore Maryland 21201 —
Nebraska Cancer Specialists (Satellite Site) Omaha Nebraska 68130-2042 —
Nebraska Cancer Specialists Omaha Nebraska 68130-2042 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
Oncology Associates of Oregon Willamette Valley Cancer Center Eugene Oregon 97401 —
Texas Oncology Dfw Dallas Texas 75231-7001 —
Texas Oncology Tyler Tyler Texas 75702-7522 —
Utah Cancer Specialists Cancer Center Salt Lake City Utah 84107 —

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 21 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT06637501, 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 Jul 9, 2026 · Synced Nov 1, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT06637501 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →