drugset / Trial / NCT04260217

APG-2575 Single Agent or in Combination With Ibrutinib or Rituximab in Patients With Waldenström Macroglobulinemia

NCT04260217

Phase 1 Completed 46 enrolled Ascentage Pharma Group Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

Phase Ib/II study of safety, tolerability, efficacy and PK of APG-2575 as a single agent or in combination with other therapeutic agents including ibrutinib or rituximab.

Timeline

Start
2021-05-30
Primary completion
2024-02-05
Completion
2025-08-13

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