vasopharm's Traumatic Brain Injury Drug Exceeds Expectations in Phase IIa Exploratory Clinical Trial

WUERZBURG, Germany, September 17, 2012 /PRNewswire/ --

VAS203 demonstrates potential as safe and effective treatment

vasopharm GmbH, a pharmaceutical company dedicated to the discovery and development of novel therapeutics for the treatment of cerebro- and cardiovascular diseases, today announces that the explorative phase IIa NOSTRA trial in Traumatic Brain Injury Patients met all clinical endpoints for safety and in addition demonstrated strong evidence of clinical benefit in patients.

Traumatic Brain Injury is caused when an external force impacts the head. It is a condition with high unmet medical need and is the leading cause of death and disability among young adults in the developed world. TBI accounts for more potential years of life lost than cancer and cardiovascular disease combined and there are currently no drugs available to treat this condition.

The NOSTRA (NO-Synthase inhibition in TRAumatic brain injury) trial was a European, multicentre, placebo-controlled, double blind study with safety and tolerability as primary endpoints. The study employed 'in vivo' microdialysis to monitor pharmacodynamic and pharmacokinetic properties of the compound VAS203. VAS203 is a novel allosteric NO-synthase antagonist which interrupts the inducible nitric oxide process involved in brain swelling.

In total, 32 patients with moderate to severe traumatic brain injury were enrolled in three cohorts in six study centres in Spain, England, Austria, France and Switzerland. All study centres used continuous microdialysis to monitor cerebral energy household, NO metabolism and concentration of the drug in the brain tissue. VAS203 was administered in addition to standard of care treatment.

Highlights of the Phase IIa trial

Final analysis of the data showed that all clinical endpoints were achieved: the drug demonstrated good safety and tolerability and reached the brain tissues in pharmacologically relevant amounts. Furthermore, mortality was 12.5% in the placebo group versus no deaths in the drug group.

VAS203 did not have any negative effect on the cerebral perfusion pressure. The Therapy Intensity Level (TIL) - a marker evaluating concomitant therapy and intervention by the physicians as a measure for control of intracranial pressure (ICP) - demonstrated a substantial reduction in VAS203 treated patients compared to placebo. Interpretation of data on ICP - often used as a surrogate endpoint in TBI clinical trials - is impractical without reference to the intensity of therapy directed at controlling ICP.

In addition the extended Glasgow Outcome Scale (eGOS) was used off protocol to assess the level of achieved neurological recovery six months post-injury. In comparison to the placebo group, the eGOS determined at six months post-injury, was significantly increased demonstrating a substantially improved recovery in patients receiving VAS203 (p = 0.006).

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vasopharm's Traumatic Brain Injury Drug Exceeds Expectations in Phase IIa Exploratory Clinical Trial