RecruitingPhase 1Phase 2NCT07520006

Study of NX-5948 in Combination With Other Agents in Adults With B-cell Malignancies

An Open-label, Multicenter Phase 1b/2 Study to Evaluate the Safety and Efficacy of NX-5948 in Combination With Other Agents in Adults With B-cell Malignancies


Sponsor

Nurix Therapeutics, Inc.

Enrollment

150 participants

Start Date

Aug 1, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The study will evaluate NX-5948 (bexobrutideg) in combination with venetoclax with or without an anti-CD20 antibody (rituximab or obinutuzumab) in second-line or higher (2L+) relapsed/refractory (R/R) or first-line (1L) chronic lymphocytic leukemia (CLL)/small lymphocytic lymphoma (SLL).


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called NX-5948, a drug called obinutuzumab, and others for people with b-cell lymphoma, chronic lymphocytic leukemia, and other related conditions. The study is currently recruiting participants at 6 locations. People eligible for this study include aged 18 Years and older.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGNX-5948

Administered orally once daily as a capsule

DRUGvenetoclax

Administered orally once daily as a tablet per prescribing information

DRUGrituximab

Administered as an intravenous (IV) infusion per prescribing information

DRUGobinutuzumab

Administered as an IV infusion per prescribing information


Locations(6)

Rocky Mountain Cancer Centers

Aurora, Colorado, United States

University of Miami

Coral Gables, Florida, United States

Oncology Associates of Oregon

Eugene, Oregon, United States

UPMC Hillman Cancer Center

Pittsburgh, Pennsylvania, United States

SCRI Oncology Partners

Nashville, Tennessee, United States

Texas Oncology - Northeast

Tyler, Texas, United States

View Full Details on ClinicalTrials.gov

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NCT07520006


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