drugset / Trial / NCT06973187

A Study to Evaluate the Safety and Efficacy of BGB-16673 Compared to Pirtobrutinib in Adults With Relapsed/Refractory Chronic Lymphocytic Leukemia or Small Lymphocytic Lymphoma

NCT06973187

Phase 3 Recruiting 500 enrolled BeOne Medicines
RandomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of BGB-16673 alone compared with pirtobrutinib in patients with relapsed or refractory (R/R) chronic lymphocytic leukemia (CLL) or small lymphocytic lymphoma (SLL) who had been previously treated with a covalent Bruton tyrosine kinase inhibitor (cBTKi).

Timeline

Start
2025-09-04
Primary completion
2028-04-17
Completion
2028-04-17

Drugs

EvaluationDrugModalityDoseRoute
Subject BGB-16673 Other / unclassified Oral
Comparator Pirtobrutinib Other / unclassified Oral