A Study of NX-5948 in Adults With CLL/SLL Previously Treated With a Bruton's Tyrosine Kinase Inhibitor and a B-cell Lymphoma-2 Inhibitor (DAYBreak CLL-201)
Part of paid clinical trials in Duarte, California.
- Sponsor
- Nurix Therapeutics, Inc.
- Study ID
- NCT07221500
- Phase
- PHASE2
- Status
- Recruiting
Conditions
- Chronic Lymphocytic Leukemia (CLL)
- Small Lymphocytic Lymphoma (SLL)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- NX-5948 — DRUGOral dose administered once daily. NX-5948 will be given in continuous 28-day cycles.
Study Details
This is a study for patients with relapsed/refractory (R/R) chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) who have previously received treatment with a BTK inhibitor (covalent and non-covalent) and a BCL-2 inhibitor. The main purpose of this study is to test if NX-5948 (bexobrutideg) works to treat patients with CLL/SLL. Participation could last up to 5 years, and possibly longer, if the disease does not progress.
Key Dates
- First listed
- Oct 28, 2025
- Start date
- Oct 15, 2025
- Status verified
- Jun 2026
- Primary completion
- Jan 31, 2028
- Completion
- Oct 31, 2030
Study Design
- Enrollment
- 100 participants (estimated)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: NX-5948
Primary Outcome Measure
Objective response rate without partial response with lymphocytosis (PR-L) as determined by an Independent Review Committee (IRC) [ Time Frame: Up to approximately 5 years ]
Central Contacts
- Additional Site Contact Information415-417-3418
Locations (20)
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