drugset / Trial / NCT05053880

A Study to Evaluate Safety and Efficacy of ACT001 and Anti-PD-1 in Patients With Surgically Accessible Recurrent Glioblastoma Multiforme

NCT05053880 ↗

RandomizedSequentialOpen-labelTreatment

Summary

The current design provides a window to analyze the impact of the ACT001+Pembrolizumab combination on the tumor microenvironment and disease outcomes.

Timeline

Start
2021-09-22
Primary completion
2024-10-25
Completion
2026-12-31

Drugs

EvaluationDrugModalityDoseRoute
Subject ACT001 Unknown 200 mg Oral
Subject ACT001 Unknown 400 mg Oral
Subject ACT001 Unknown 800 mg Oral
Subject Pembrolizumab Monoclonal antibody 200 mg Intravenous

Indications