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Clinical Trial Summary

This is a global multicenter, open label, randomized, registrational phase III study to investigate the efficacy and safety of lisaftoclax in combination with BTK inhibitors in CLL/SLL patients who previously treated with BTK inhibitors


Clinical Trial Description

Approximately 440 patients will be enrolled, the patients who meet the eligibility criteria will be randomized in a 1:1 ratio to investigational arm (lisaftoclax in combination with a BTK inhibitor) or the control arm (BTK inhibitor alone). These patients with CLL/SLL have been on BTKi monotherapy and meet all other protocol required eligibility criteria. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06104566
Study type Interventional
Source Ascentage Pharma Group Inc.
Contact Laura Glass, MD
Phone 301-520-5964
Email laura.glass@ascentage.com
Status Recruiting
Phase Phase 3
Start date December 20, 2023
Completion date October 31, 2027

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