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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
