drugset / Trial / NCT07609823

A Study of Lacutoclax (LP-108) in Patients With Relapsed/Refractory CLL/SLL

NCT07609823

Phase 2 Not yet recruiting 75 enrolled Guangzhou Lupeng Pharmaceutical Company LTD.
NaSingle-groupOpen-labelTreatment

Summary

The goal of this clinical trial is to evaluate the efficacy and safety of Lacutoclax, an oral selective BCL-2 inhibitor, in patients with relapsed or refractory chronic lymphocytic leukemia/small lymphocytic lymphoma (CLL/SLL). Lacutoclax is a potent and selective BCL-2 inhibitor with relatively weaker inhibitory activity against BCL-XL and BCL-W. Preliminary clinical data have demonstrated promising efficacy and an acceptable safety profile in patients with CLL/SLL and other B-cell non-Hodgkin lymphomas (B-NHLs). This is an open-label, single-arm, multicenter Phase II study evaluating the efficacy and safety of oral Lacutoclax tablets in patients with relapsed or refractory CLL/SLL.

Timeline

Start
2026-07-30
Primary completion
2028-03-30
Completion
2029-09-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Lacutoclax Small molecule 400 mg Oral