drugset / Trial / NCT07609862

A Study of Rocbrutinib in Combination With Lacutoclax in Patients With B-Cell Malignancies

NCT07609862

Phase 1/2 Not yet recruiting 92 enrolled Guangzhou Lupeng Pharmaceutical Company LTD.
NaSingle-groupOpen-labelTreatment

Summary

BTK inhibitors and BCL-2 inhibitors have demonstrated significant clinical activity in mature B-cell malignancies, and combination therapy may provide improved clinical benefit. This is a multi-center, open-label, single-arm Phase Ib/II clinical study. The purpose of this clinical trial is to investigate the safety, tolerability, pharmacokinetics, and preliminary efficacy of Rocbrutinib, a fourth-generation Bruton tyrosine kinase inhibitor (BTKi), in combination with the BCL-2 inhibitor Lacutoclax in patients with mature B-cell malignancies. The Phase Ib will use a classic 3+3 dose-escalation design to evaluate dose-limiting toxicities (DLTs), determine the maximum tolerated dose (MTD), and identify the recommended dosing regimen. The Phase II portion is intended to further evaluate the efficacy and safety of the combination therapy.

Timeline

Start
2026-05-30
Primary completion
2029-06-30
Completion
2033-05-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Lacutoclax Small molecule 200 mg
Subject Lacutoclax Small molecule 400 mg
Subject Rocbrutinib Small molecule 150 mg