Detailed Info
Brief 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.
Study Phase
Phase 1/Phase 2
Estimated Enrollment
55
Estimated Primary Completion Date
December 2015
Study Type
Interventional
Interventions
- Drug: VAL-083 (Dianhydrogalactitol)
Sponsor
DelMar Pharmaceuticals, Inc.