drugset / Trial / NCT04215809

Study of APG-2575 as a Single Agent or in Combination With Other Therapeutic Agents for CLL/SLL

NCT04215809

Phase 1 Recruiting 144 enrolled Ascentage Pharma Group Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Assess the safety and tolerability, identify dose-limiting toxicities (DLT) and determine the maximum tolerated dose (MTD) / recommended phase 2 dose (RP2D) of lisaftoclax.

Timeline

Start
2020-03-02
Primary completion
2025-10-31
Completion
2027-06-30

Drugs

EvaluationDrugModalityDoseRoute
Subject APG-2575 Small molecule 400 mg Oral
Subject APG-2575 Small molecule 600 mg Oral
Subject APG-2575 Small molecule 800 mg Oral
Subject APG-2575 Small molecule 1000 mg Oral