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A novel therapy for Glioblastoma, the most common and most malignant form of brain tumor

Reference number
Coordinator Glionova AB
Funding from Vinnova SEK 4 950 000
Project duration January 2015 - December 2016
Status Completed

Purpose and goal

The concrete goal with this project is to compile a full GLP safety pharmacology and toxicology package for our candidate drug GLN-1001 (Vacquinol-1), in accordance with the regulatory requirements and therein to document an acceptable safety profile, justifying clinical trials with the intended doses.

Expected results and effects

The results of safety pharmacology and toxicological testing and further efficacy studies do not enable the start of clinical Phase I/II and proof of concept studies in patients.

Planned approach and implementation

A full GLP safety pharmacology and toxicology package in accordance with the regulatory requirements has been completed on time and on budget, involving internal resources as well as external CROs, Karolinska Institutet and Mayo Clinic.

External links

The project description has been provided by the project members themselves and the text has not been looked at by our editors.

Last updated 25 November 2019

Reference number 2014-04663

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