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Clinical Trial Summary

This is a global, multicenter, randomized, open-label, Phase III confirmatory study to investigate the efficacy and safety of Lisaftoclax (APG-2575) in combination with Acalabrutinib in patients with newly diagnosed CLL/SLL.


Clinical Trial Description

The patients with newly diagnosed CLL/SLL, who have met all required eligibility criteria, will be randomized to the investigational group (Lisaftoclax in combination with Acalabrutinib) or the control group (immunochemotherapy, CIT). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06319456
Study type Interventional
Source Ascentage Pharma Group Inc.
Contact Yifan Zhai, M.D., Ph.D.
Phone +86-20-28068501
Email yzhai@ascentage.com
Status Recruiting
Phase Phase 3
Start date April 7, 2024
Completion date August 2028

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