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

Primary Purpose

Traumatic Brain Injury

Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
VAS203
Saline
Sponsored by
veriNOS operations GmbH
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Traumatic Brain Injury

Eligibility Criteria

18 Years - 60 Years (Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Written informed consent from patient's legal guardian or legal representative or deferred 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 earlier than 6 hours after the injury)
  5. TBI with Glasgow Coma Score (GCS) ≥ 3 requiring intracranial pressure (ICP) monitoring according to the assessment of the treating physician.
  6. Catheter placement (intraventricular or intraparenchymal, only) for monitoring and management of increased ICP
  7. Systolic blood pressure ≥ 100 mmHg
  8. Females of child-bearing potential must have a negative pregnancy test

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 causing continuing bleeding likely to require multiple transfusions (> 4 units red blood cells)
  5. Coma due to an exclusive epidural hematoma (lucid interval and absence of structural brain damage on CT scan)
  6. Coma suspected to be primarily due to other causes than head injury (e.g. drug overdose 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, or French, 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 Chronic Kidney 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, coronary disease; major psychiatric disorder; alcohol or drug abuse), that can be ascertained at admission
  18. Known to have received an experimental drug within 4 weeks prior to current injury

Sites / Locations

  • Universitätsklinik für Neurochirurgie
  • Neurologie und Neurochirurgie Medizinische Universität Innsbruck
  • Klinik für Allgemeine Anästhesie und Intensivmedizin AKH Wien
  • Hôpital Pellegrin Service de réanimation traumatologique et chirurgicale
  • Hopital Gabriel Montpied
  • Pôle Anesthésie Réanimation Douleur Urgence
  • HIA Sainte-Anne Boulevard Sainte-Anne
  • Charite Virchow-Klinikum
  • Berufsgenossenschaftliche Kliniken Bergmannsheil Klinik für Neurochirurgie
  • Allgemeines Krankenhaus Celle Neurotraumatologie
  • Universitätsklinikum Düsseldorf Neurochirurgische Klinik
  • Klinik für Neurochirurgie Universität Frankfurt
  • Universitätsklinikum Göttingen Klinik für Neurochirurgie
  • Berufsgenossenschaftliche Kliniken Bergmannstrost Halle Klinik für Neurochirurgie
  • Universitätsklinikum Hamburg-Eppendorf Klinik und Poliklinik für Neurochirurgie
  • Medizinische Hochschule Hannover Klinik für Neurochirurgie
  • Neurochirurgische Universitätsklinik Heidelberg
  • Universitätsklinikum des Saarlands
  • Universitätsklinikum Jena Klinik und Poliklinik für Neurochirurgie
  • Universitätsklinikum Schleswig-Holstein Klinik für Neurochirurgie
  • Universitätsklinikum Leipzig Klinik und Poliklinik für Neurochirurgie
  • Vall d'Hebron University Hospital Department of Neurosurgery
  • Hospital General Universitario
  • Hospital 12 de Octubre
  • Son Espases University Hospital
  • Queen Elizabeth Hospital Birmingham
  • NHS Lothian University of Edinburgh
  • Kings College Hospital London
  • Southampton University Hospital Division of Clinical Neurosciences

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

VAS203 (Ronopterin)

Saline

Arm Description

Intravenous infusion of 17 mg/kg VAS203 over 48 hours, daily dose 8.5 mg/kg

Intravenous infusion of physiological saline over 48 hours

Outcomes

Primary Outcome Measures

extended Glasgow Outcome Scale
clinical outcome questionnaire

Secondary Outcome Measures

Quality of life after brain injury (QOLIBRI)
clinical outcome questionnaire
QOLIBRI overall scale
clinical outcome questionnaire
extended Glasgow Outcome Scale
clinical outcome questionnaire
QOLIBRI overall scale
clinical outcome questionnaire
Therapy Intensity Level
Daily recording of score for therapeutic measures
Number of decompressive craniectomies
Number of decompressive craniotomies on both hemispheres

Full Information

First Posted
May 31, 2016
Last Updated
October 6, 2021
Sponsor
veriNOS operations GmbH
Collaborators
ICON plc
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1. Study Identification

Unique Protocol Identification Number
NCT02794168
Brief Title
Efficacy of VAS203 (Ronopterin) in Patients With Moderate and Severe Traumatic Brain Injury
Acronym
NOSTRA-III
Official Title
Efficacy of VAS203 (Ronopterin) in Patients With Moderate and Severe Traumatic Brain Injury - (NOSTRA Phase III Trial): A Confirmatory, Placebo-controlled, Randomised, Double Blind, Multi-centre Study
Study Type
Interventional

2. Study Status

Record Verification Date
October 2021
Overall Recruitment Status
Completed
Study Start Date
June 2016 (Actual)
Primary Completion Date
June 30, 2020 (Actual)
Study Completion Date
June 30, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
veriNOS operations GmbH
Collaborators
ICON plc

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief 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.
Detailed 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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Traumatic Brain Injury

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
224 (Actual)

8. Arms, Groups, and Interventions

Arm Title
VAS203 (Ronopterin)
Arm Type
Experimental
Arm Description
Intravenous infusion of 17 mg/kg VAS203 over 48 hours, daily dose 8.5 mg/kg
Arm Title
Saline
Arm Type
Placebo Comparator
Arm Description
Intravenous infusion of physiological saline over 48 hours
Intervention Type
Drug
Intervention Name(s)
VAS203
Other Intervention Name(s)
Ronopterin
Intervention Description
Treatment
Intervention Type
Drug
Intervention Name(s)
Saline
Intervention Description
Placebo
Primary Outcome Measure Information:
Title
extended Glasgow Outcome Scale
Description
clinical outcome questionnaire
Time Frame
6 months
Secondary Outcome Measure Information:
Title
Quality of life after brain injury (QOLIBRI)
Description
clinical outcome questionnaire
Time Frame
6 months
Title
QOLIBRI overall scale
Description
clinical outcome questionnaire
Time Frame
6 months
Title
extended Glasgow Outcome Scale
Description
clinical outcome questionnaire
Time Frame
3 months
Title
QOLIBRI overall scale
Description
clinical outcome questionnaire
Time Frame
3 months
Title
Therapy Intensity Level
Description
Daily recording of score for therapeutic measures
Time Frame
14 days
Title
Number of decompressive craniectomies
Description
Number of decompressive craniotomies on both hemispheres
Time Frame
14 days
Other Pre-specified Outcome Measures:
Title
Adverse Events
Description
Number of adverse events related to treatment
Time Frame
14 days
Title
Renal function
Description
Number of patients exhibiting acute kidney injury according Acute Kidney Injury Network criteria
Time Frame
14 days
Title
Mortality
Description
Mortality 6 months after traumatic brain injury
Time Frame
6 Months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
60 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Written informed consent from patient's legal guardian or legal representative or deferred consent procedure, according to local requirements 18 - 60 years of age, inclusive Expected to survive more than 24 hours after admission Traumatic Brain Injury (TBI) within the last 18 hours (infusion must not start earlier than 6 hours after the injury) TBI with Glasgow Coma Score (GCS) ≥ 3 requiring intracranial pressure (ICP) monitoring according to the assessment of the treating physician. Catheter placement (intraventricular or intraparenchymal, only) for monitoring and management of increased ICP Systolic blood pressure ≥ 100 mmHg Females of child-bearing potential must have a negative pregnancy test Exclusion Criteria: Penetrating head injury (e.g. missile, stab wound) Concurrent, but not pre-existing, spinal cord injury Bilateral fixed and dilated pupil (> 4 mm) Cardiopulmonary resuscitation performed post injury, or extracranial injuries causing continuing bleeding likely to require multiple transfusions (> 4 units red blood cells) Coma due to an exclusive epidural hematoma (lucid interval and absence of structural brain damage on CT scan) Coma suspected to be primarily due to other causes than head injury (e.g. drug overdose intoxication, drowning/near drowning) Known or CT scan evidence of pre-existing major cerebral damage Patients who cannot be monitored with regard to their recovery (eGOS-I and QOLIBRI) Patients and relatives of patients who don´t understand/speak Spanish, or English, or French, or German Decompressive craniectomy, planned prior to randomisation Polytraumatic patients with Injury Severity Score non-head > 18 Rhabdomyolysis with Creatine Kinase > 5000 IU/L Injuries to ascending aorta and/or carotid arteries and vertebral arteries Serum creatinine values > 1.2 mg/dL (106 µmol/L) (women), or > 1.5 mg/dL (133 µmol/L) (men) Estimated glomerular filtration rate (eGFR) < 60 mL/min as calculated by Chronic Kidney Disease Epidemiology Collaboration Formula BMI < 18.5 kg/m2 and > 40 kg/m2, Body weight > 110 kg Any severe concomitant condition (cancer; hematologic, renal, hepatic, coronary disease; major psychiatric disorder; alcohol or drug abuse), that can be ascertained at admission Known to have received an experimental drug within 4 weeks prior to current injury
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Erich Schmutzhard, Prof. MD
Organizational Affiliation
Medical University Innsbruck
Official's Role
Principal Investigator
Facility Information:
Facility Name
Universitätsklinik für Neurochirurgie
City
Graz
ZIP/Postal Code
8036
Country
Austria
Facility Name
Neurologie und Neurochirurgie Medizinische Universität Innsbruck
City
Innsbruck
Country
Austria
Facility Name
Klinik für Allgemeine Anästhesie und Intensivmedizin AKH Wien
City
Wien
Country
Austria
Facility Name
Hôpital Pellegrin Service de réanimation traumatologique et chirurgicale
City
Bordeaux
ZIP/Postal Code
33076
Country
France
Facility Name
Hopital Gabriel Montpied
City
Clermont-Ferrand
ZIP/Postal Code
63003
Country
France
Facility Name
Pôle Anesthésie Réanimation Douleur Urgence
City
Nimes
Country
France
Facility Name
HIA Sainte-Anne Boulevard Sainte-Anne
City
Toulon
ZIP/Postal Code
83800
Country
France
Facility Name
Charite Virchow-Klinikum
City
Berlin
ZIP/Postal Code
13353
Country
Germany
Facility Name
Berufsgenossenschaftliche Kliniken Bergmannsheil Klinik für Neurochirurgie
City
Bochum
Country
Germany
Facility Name
Allgemeines Krankenhaus Celle Neurotraumatologie
City
Celle
Country
Germany
Facility Name
Universitätsklinikum Düsseldorf Neurochirurgische Klinik
City
Düsseldorf
Country
Germany
Facility Name
Klinik für Neurochirurgie Universität Frankfurt
City
Frankfurt
Country
Germany
Facility Name
Universitätsklinikum Göttingen Klinik für Neurochirurgie
City
Göttingen
Country
Germany
Facility Name
Berufsgenossenschaftliche Kliniken Bergmannstrost Halle Klinik für Neurochirurgie
City
Halle
Country
Germany
Facility Name
Universitätsklinikum Hamburg-Eppendorf Klinik und Poliklinik für Neurochirurgie
City
Hamburg
Country
Germany
Facility Name
Medizinische Hochschule Hannover Klinik für Neurochirurgie
City
Hannover
Country
Germany
Facility Name
Neurochirurgische Universitätsklinik Heidelberg
City
Heidelberg
Country
Germany
Facility Name
Universitätsklinikum des Saarlands
City
Homburg
ZIP/Postal Code
66421
Country
Germany
Facility Name
Universitätsklinikum Jena Klinik und Poliklinik für Neurochirurgie
City
Jena
Country
Germany
Facility Name
Universitätsklinikum Schleswig-Holstein Klinik für Neurochirurgie
City
Kiel
Country
Germany
Facility Name
Universitätsklinikum Leipzig Klinik und Poliklinik für Neurochirurgie
City
Leipzig
Country
Germany
Facility Name
Vall d'Hebron University Hospital Department of Neurosurgery
City
Barcelona
ZIP/Postal Code
08035
Country
Spain
Facility Name
Hospital General Universitario
City
Elche
Country
Spain
Facility Name
Hospital 12 de Octubre
City
Madrid
Country
Spain
Facility Name
Son Espases University Hospital
City
Palma
Country
Spain
Facility Name
Queen Elizabeth Hospital Birmingham
City
Birmingham
Country
United Kingdom
Facility Name
NHS Lothian University of Edinburgh
City
Edinburgh
Country
United Kingdom
Facility Name
Kings College Hospital London
City
London
Country
United Kingdom
Facility Name
Southampton University Hospital Division of Clinical Neurosciences
City
Southampton
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
24831445
Citation
Stover JF, Belli A, Boret H, Bulters D, Sahuquillo J, Schmutzhard E, Zavala E, Ungerstedt U, Schinzel R, Tegtmeier F; NOSTRA Investigators. Nitric oxide synthase inhibition with the antipterin VAS203 improves outcome in moderate and severe traumatic brain injury: a placebo-controlled randomized Phase IIa trial (NOSTRA). J Neurotrauma. 2014 Oct 1;31(19):1599-606. doi: 10.1089/neu.2014.3344. Epub 2014 Jul 28.
Results Reference
background
PubMed Identifier
31937347
Citation
Tegtmeier F, Schinzel R, Beer R, Bulters D, LeFrant JY, Sahuquillo J, Unterberg A, Andrews P, Belli A, Ibanez J, Lagares A, Mokry M, Willschke H, Fluh C, Schmutzhard E; NOSTRA Investigators. Efficacy of Ronopterin (VAS203) in Patients with Moderate and Severe Traumatic Brain Injury (NOSTRA phase III trial): study protocol of a confirmatory, placebo-controlled, randomised, double blind, multi-centre study. Trials. 2020 Jan 14;21(1):80. doi: 10.1186/s13063-019-3965-4. Erratum In: Trials. 2020 Feb 12;21(1):172.
Results Reference
derived

Learn more about this trial

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

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