Clinical Trial

Trial Protocol ID USOR 24268: 2L+ R/R CLL/SLL Ph2 study to evaluate NX-5948 in adults with CLL or SLL exposed to BTKi and BCL-2i

Trial Description

NX-5948-201: 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)

MOA: NX-5948 (bexobrutideg) is a CTM that induces the degradation of BTK in cells through recruitment of CRBN and promotes the formation of a ternary complex of CRBN, NX-5948, and BTK.

Key Eligibility Criteria:

  • Confirmed diagnosis of relapsed/refractory CLL/SLL
  • ECOG ≤2
  • Subjects must have prior exposure to a cBTKi, ncBTKi, and BCL-2i either in separate LOT or in combination
  • Subjects must have measurable disease by CT
  • Subjects previously treated with a BTK degrader are excluded
  • Subjects with a known or suspected prolymphocytic
    leukemia or Richter’s transformation are excluded

Contact us regarding Clinical Trials at MOHRSCH@usoncology.com or call us at 877-664-7724

Investigator

  • Mohit Narang, MD

Sponsor

  • Nurix Therapeutics, Inc.

ClinicalTrials.gov NCT ID

  • NCT07221500