drugset / Trial / NCT05540275

Tislelizumab (One Anti-PD-1 Antibody) Plus Low-dose Bevacizumab for Bevacizumab Refractory Recurrent Glioblastoma

NCT05540275 ↗

Phase 2 Not yet recruiting 30 enrolled Henan Provincial People's Hospital
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the clinical efficacy and safety of Tislelizumab (one anti-PD-1 antibody same as nivolumab approved in China) in combination with bevacizumab in patients with recurrent or progressive glioblastoma (GBM) who have progressed on bevacizumab with or without PTEN or TERT gene mutations.

Timeline

Start
2023-10-05
Primary completion
2024-12
Completion
2026-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 3 mg/kg —
Subject Tislelizumab Monoclonal antibody 200 mg —

Indications