A Single-arm, Phase 2, Open-label, Multicenter Study to Evaluate NX-5948 in Adults With Relapsed/Refractory (R/R) Chronic Lymphocytic Leukemia (CLL) or Small Lymphocytic Lymphoma (SLL) Previously Exposed to a Bruton's Tyrosine Kinase Inhibitor (BTKi) and a B-cell Lymphoma-2 Inhibitor (BCL-2i)

Status: Recruiting
Location: See all (6) locations...
Intervention Type: Drug
Study Type: Interventional
Study Phase: Phase 2
SUMMARY

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 and a BCL-2 inhibitor. The main purpose of this study is to test if NX-5948 works to treat patients with CLL/SLL. Participation could last up to 5 years, and possibly longer, if the disease does not progress.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Age: ≥ 18 years

• Confirmed relapsed/refractory CLL/SLL that meets iwCLL criteria for systemic treatment

• Eastern Cooperative Oncology Group (ECOG) performance status of 0-2

• Must have received both a BTK inhibitor and a BCL-2 inhibitor

• Measurable disease by radiographic assessment

• Adequate organ and bone marrow function

• Must sign an informed consent form indicating that he or she understands the purpose of the procedures required for the study and is willing to participate

Locations
Other Locations
France
CHU de Nantes
RECRUITING
Nantes
Poland
Pratia Hematologia Sp. z o.o.
RECRUITING
Katowice
Pratia S.A.
RECRUITING
Krakow
Aidport Sp. z o.o.
RECRUITING
Skorzewo
United Kingdom
The Royal Marsden NHS Foundation Trust
RECRUITING
London
The Christie NHS Foundation Trust
RECRUITING
Manchester
Contact Information
Primary
Additional Site Contact Information
clinicaltrials@nurixtx.com
415-417-3418
Time Frame
Start Date: 2025-10-15
Estimated Completion Date: 2030-10
Participants
Target number of participants: 100
Treatments
Experimental: NX-5948
Sponsors
Leads: Nurix Therapeutics, Inc.

This content was sourced from clinicaltrials.gov

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