CompletedPhase 2NCT02012582
Phase 2 a Study to Assess Safety and Pharmacokinetics of VAS203 in Patients With Traumatic Brain Injury
Studying Moderate and severe traumatic brain injury
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- veriNOS operations GmbH
- Principal Investigator
- Frank Tegtmeier, Dr.veriNOS operations GmbH
- Intervention
- VAS203(drug)
- Enrollment
- 32 target
- Eligibility
- 18-65 years · All sexes
- Timeline
- 2009 – 2012
Study locations (6)
- Medical University Innsbruck Department of Neurology, Innsbruck, Austria
- HIA Sainte-Anne Boulevard Sainte-Anne, Toulon, France
- Vall d'Hebron University Hospital Department of Neurosurgery, Barcelona, Spain
- Hospital Clinic University of Barcelona Surgical Intensive Care Unit, Barcelona, Spain
- University Hospital Zuerich Surgical Intensive Care, Zurich, Switzerland
- Southampton University Hospital Division of Clinical Neurosciences, Southampton, United Kingdom
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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