Efficacy of VAS203 (Ronopterin) in Patients With Moderate and Severe Traumatic Brain Injury

Last updated: October 6, 2021
Sponsor: Vasopharm GmbH
Overall Status: Completed

Phase

3

Condition

Memory Loss

Neurologic Disorders

Traumatic Brain Injury

Treatment

N/A

Clinical Study ID

NCT02794168
VAS203/III/1/04
  • Ages 18-60
  • All Genders

Study Summary

This study evaluates the efficacy of an infusion of Ronopterin (VAS203) on clinical outcome in patients with moderate and severe traumatic brain injury. Half of the participants will receive Ronopterin (VAS203), while the other half will receive placebo.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  1. Written informed consent from patient's legal guardian or legal representative ordeferred consent procedure, according to local requirements
  2. 18 - 60 years of age, inclusive
  3. Expected to survive more than 24 hours after admission
  4. Traumatic Brain Injury (TBI) within the last 18 hours (infusion must not start earlierthan 6 hours after the injury)
  5. TBI with Glasgow Coma Score (GCS) ≥ 3 requiring intracranial pressure (ICP) monitoringaccording to the assessment of the treating physician.
  6. Catheter placement (intraventricular or intraparenchymal, only) for monitoring andmanagement of increased ICP
  7. Systolic blood pressure ≥ 100 mmHg
  8. Females of child-bearing potential must have a negative pregnancy test

Exclusion

Exclusion Criteria:

  1. Penetrating head injury (e.g. missile, stab wound)
  2. Concurrent, but not pre-existing, spinal cord injury
  3. Bilateral fixed and dilated pupil (> 4 mm)
  4. Cardiopulmonary resuscitation performed post injury, or extracranial injuries causingcontinuing bleeding likely to require multiple transfusions (> 4 units red bloodcells)
  5. Coma due to an exclusive epidural hematoma (lucid interval and absence of structuralbrain damage on CT scan)
  6. Coma suspected to be primarily due to other causes than head injury (e.g. drugoverdose intoxication, drowning/near drowning)
  7. Known or CT scan evidence of pre-existing major cerebral damage
  8. Patients who cannot be monitored with regard to their recovery (eGOS-I and QOLIBRI)
  9. Patients and relatives of patients who don´t understand/speak Spanish, or English, orFrench, or German
  10. Decompressive craniectomy, planned prior to randomisation
  11. Polytraumatic patients with Injury Severity Score non-head > 18
  12. Rhabdomyolysis with Creatine Kinase > 5000 IU/L
  13. Injuries to ascending aorta and/or carotid arteries and vertebral arteries
  14. Serum creatinine values > 1.2 mg/dL (106 µmol/L) (women), or > 1.5 mg/dL (133 µmol/L) (men)
  15. Estimated glomerular filtration rate (eGFR) < 60 mL/min as calculated by ChronicKidney Disease Epidemiology Collaboration Formula
  16. BMI < 18.5 kg/m2 and > 40 kg/m2, Body weight > 110 kg
  17. Any severe concomitant condition (cancer; hematologic, renal, hepatic, coronarydisease; major psychiatric disorder; alcohol or drug abuse), that can be ascertainedat admission
  18. Known to have received an experimental drug within 4 weeks prior to current injury

Study Design

Total Participants: 224
Study Start date:
June 01, 2016
Estimated Completion Date:
June 30, 2020

Study Description

Severe and moderate traumatic brain injury (TBI) constitutes a major health problem. TBI is the leading cause of death and disability among young adults in developed countries, and the incidence in the elderly population is increasing.

Neurological damage after TBI is caused not only by the accident itself, but evolves afterwards. The posttraumatic secondary injury includes - among others - inflammation and oedema formation with subsequent increase of intracranial pressure. A key molecule in these processes is the gas nitric oxide, which is produced in excess during neuroinflammation.

Ronopterin (VAS203) is an inhibitor of nitric oxide synthase. Ronopterin reduces excess nitric oxide production and subsequent secondary injury.

Connect with a study center

  • Universitätsklinik für Neurochirurgie

    Graz, 8036
    Austria

    Site Not Available

  • Neurologie und Neurochirurgie Medizinische Universität Innsbruck

    Innsbruck,
    Austria

    Site Not Available

  • Klinik für Allgemeine Anästhesie und Intensivmedizin AKH Wien

    Wien,
    Austria

    Site Not Available

  • Hôpital Pellegrin Service de réanimation traumatologique et chirurgicale

    Bordeaux, 33076
    France

    Site Not Available

  • CHU Caen

    Caen,
    France

    Site Not Available

  • Hopital Gabriel Montpied

    Clermont-Ferrand, 63003
    France

    Site Not Available

  • Hôpital Pierre Wertheimer,

    Lyon,
    France

    Site Not Available

  • Pôle Anesthésie Réanimation Douleur Urgence

    Nimes,
    France

    Site Not Available

  • CHU Reims

    Reims,
    France

    Site Not Available

  • HIA Sainte-Anne Boulevard Sainte-Anne

    Toulon, 83800
    France

    Site Not Available

  • Charite Virchow-Klinikum

    Berlin, 13353
    Germany

    Site Not Available

  • Berufsgenossenschaftliche Kliniken Bergmannsheil Klinik für Neurochirurgie

    Bochum,
    Germany

    Site Not Available

  • Allgemeines Krankenhaus Celle Neurotraumatologie

    Celle,
    Germany

    Site Not Available

  • Universitätsklinikum Düsseldorf Neurochirurgische Klinik

    Düsseldorf,
    Germany

    Site Not Available

  • Klinik für Neurochirurgie Universität Frankfurt

    Frankfurt,
    Germany

    Site Not Available

  • Universitätsklinikum Göttingen Klinik für Neurochirurgie

    Göttingen,
    Germany

    Site Not Available

  • Berufsgenossenschaftliche Kliniken Bergmannstrost Halle Klinik für Neurochirurgie

    Halle,
    Germany

    Site Not Available

  • Universitätsklinikum Hamburg-Eppendorf Klinik und Poliklinik für Neurochirurgie

    Hamburg,
    Germany

    Site Not Available

  • Medizinische Hochschule Hannover Klinik für Neurochirurgie

    Hannover,
    Germany

    Site Not Available

  • Neurochirurgische Universitätsklinik Heidelberg

    Heidelberg,
    Germany

    Site Not Available

  • Universitätsklinikum des Saarlands

    Homburg, 66421
    Germany

    Site Not Available

  • Universitätsklinikum Jena Klinik und Poliklinik für Neurochirurgie

    Jena,
    Germany

    Site Not Available

  • Universitätsklinikum Schleswig-Holstein Klinik für Neurochirurgie

    Kiel,
    Germany

    Site Not Available

  • Universitätsklinikum Leipzig Klinik und Poliklinik für Neurochirurgie

    Leipzig,
    Germany

    Site Not Available

  • Universitätsklinik Münster

    Münster, 48149
    Germany

    Site Not Available

  • Universitätsklinikum Regensburg Klinik und Poliklinik für Neurochirurgie

    Regensburg,
    Germany

    Site Not Available

  • Universitätsmedizin Rostock Abteilung für Neurochirurgie

    Rostock,
    Germany

    Site Not Available

  • Universitätsklinikum Würzburg Klinik und Poliklinik für Neurochirurgie

    Würzburg,
    Germany

    Site Not Available

  • Vall d'Hebron University Hospital Department of Neurosurgery

    Barcelona, 08035
    Spain

    Site Not Available

  • Hospital General Universitario

    Elche,
    Spain

    Site Not Available

  • Hospital 12 de Octubre

    Madrid,
    Spain

    Site Not Available

  • Son Espases University Hospital

    Palma,
    Spain

    Site Not Available

  • Son Espases University Hospital

    Palma de Mallorca,
    Spain

    Site Not Available

  • Hospital Universitario Virgen del Rocío

    Sevilla,
    Spain

    Site Not Available

  • Hospital Clinico Universitario de Valencia Department of Anesthesiology and Critical Care

    Valencia, 46010
    Spain

    Site Not Available

  • Queen Elizabeth Hospital Birmingham

    Birmingham,
    United Kingdom

    Site Not Available

  • NHS Lothian University of Edinburgh

    Edinburgh,
    United Kingdom

    Site Not Available

  • Kings College Hospital London

    London,
    United Kingdom

    Site Not Available

  • Southampton University Hospital Division of Clinical Neurosciences

    Southampton,
    United Kingdom

    Site Not Available

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