Overview

Safety Study of VAL-083 in Patients With Recurrent Malignant Glioma

Status:
Completed
Trial end date:
2016-10-01
Target enrollment:
Participant gender:
Summary
The purpose of this Phase 1/2, open-label, single-arm study is to determine the safety and the maximal tolerated dose (MTD) of VAL-083 in patients with recurrent malignant glioma. Pharmacokinetic (PK) properties will be explored and tumor responses to treatment will be evaluated.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
DelMar Pharmaceuticals, Inc.
Treatments:
Bevacizumab
Dianhydrogalactitol
Temozolomide