drugset / Trial / NCT02336165

Phase 2 Study of Durvalumab (MEDI4736) in Patients With Glioblastoma

NCT02336165 ↗

Non-randomizedParallel-groupOpen-labelTreatment

Summary

This is an ongoing Phase 2, open-label, multicenter, non-randomized study of MEDI4736 (durvalumab) in subjects with glioblastoma (GBM) enrolled into 5 non-comparative cohorts. Primary study objectives, which vary by cohort due to differences in subject populations, include evaluation of the clinical efficacy as measured by the overall survival (OS) rate at 12 months (Cohort A), progression-free survival (PFS) at 6 months (Cohorts B, B2, and B3), and OS at 6 months (Cohort C). For all cohorts, secondary objectives include evaluation of the safety/tolerability and clinical efficacy of study treatment, and exploratory objectives include evaluation of the neurologic function and correlative biomarkers.

Timeline

Start
2015-02-26
Primary completion
2018-11
Completion
2021-07-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Bevacizumab Monoclonal antibody 3 mg/kg Intravenous
Subject Bevacizumab Monoclonal antibody 10 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 1 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 3 mg/kg Intravenous
Subject Durvalumab Monoclonal antibody 10 mg/kg Intravenous

Indications