| Indication | Chronic Lymphocytic Leukemia |
| Drug | bexobrutideg |
| Mechanism of Action | Bruton’s tyrosine kinase (BTK) degrader |
| Company | Nurix Therapeutics, Inc. |
| Trial Phase | Phase 1b/2 |
| Trial Acronym | NX-5948-203 |
| NCT ID | NCT07520006 |
| Category | Clinical Trial Event |
| Sub Category | Trial Initiation / First Patient In (FPI) |
| Therapeutic Area | Oncology |
| Combination Partner | venetoclax |
| Collaboration Partner | Roche |
| Combination Partner Class | BCL2 inhibitor |
| Patient Subpopulation | relapsed/refractory CLL, treatment-naïve CLL |
| Future Combination Partners | rituximab, obinutuzumab |
| Press Release Date | October 06, 2026 |
| Drug Characteristics | oral, brain-penetrant |
| Other Clinical Trials | DAYBreak CLL-201 (NCT07221500), DAYBreak CLL-306 (NCT07516093), NX-5948-301 (NCT05131022) |
Nurix Enrolls First Patient in Bexobrutideg/Venetoclax CLL Study
Nurix Therapeutics announced the enrollment of the first patient in its Phase 1b/2 NX-5948-203 study. This trial evaluates bexobrutideg, an investigational oral Bruton’s tyrosine kinase (BTK) degrader, in combination with venetoclax, a standard-of-care BCL2 inhibitor, for patients with chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). The initial cohort focuses on relapsed/refractory CLL, with potential expansion to first-line CLL and other B-cell malignancies. The study, conducted under a global collaboration with Roche, aims to assess safety, tolerability, and clinical activity to inform future registrational development strategies.
- The NX-5948-203 study is a Phase 1b/2 trial designed to evaluate the safety, tolerability, and clinical activity of bexobrutideg in combination with venetoclax. It initially targets relapsed/refractory CLL/SLL patients, with plans to expand to first-line CLL and potentially other B-cell malignancies. The data from this trial are crucial for informing future registrational development strategies across various lines of therapy in CLL.
- Bexobrutideg is highlighted as an investigational oral, brain-penetrant, highly selective BTK degrader with a differentiated mechanism of action. Its robust single-agent activity and favorable tolerability make it an attractive candidate for combination approaches, aiming to deliver deep, durable responses with fixed-duration therapy in B-cell malignancies.
- This combination study is part of a comprehensive clinical development program for bexobrutideg. Other ongoing trials include the pivotal single-arm Phase 2 DAYBreak CLL-201 study in relapsed/refractory CLL, the randomized Phase 3 DAYBreak CLL-306 trial comparing it to pirtobrutinib, and the Phase 1a/1b NX-5948-301 study in relapsed/refractory B-cell malignancies.
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