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CompletedNCT00190047Updated Nov 26, 2007

Effects Of DP-b99 On Neurological Function In Subjects With Acute Ischemic Hemispheric Stroke

A Phase 2 interventional study of DP-b99 in Brain Ischemia, Stroke and Cerebrovascular Disorders, sponsored by D-Pharm Ltd.. Completed at 22 sites in 2 countries. Open to participants aged 18 Years to 85 Years. Per ClinicalTrials.gov, last updated 2007-11-26.

Sponsored by D-Pharm Ltd. · Phase 2, Interventional, and Treatment

Phase
Phase 2
Study type
Interventional
Enrollment
150
Allocation
Randomized
Ages
18 Years to 85 Years
Sex
All
01

Study summary

This study will examine if DP-b99 can improve neurological function (for example strength and coordination) in the 3 months after an acute stroke

Read the detailed description

The study will include a Screening/Baseline Period, a Treatment Period, and a Post-treatment Follow-up Period. During the Screening Period, subjects will be selected for the study on the basis of inclusion and exclusion criteria (see below). A screening computed tomography scan to exclude brain bleeding will be performed. The patient's informed consent will be obtained. The patient will be randomly allocated to DP-b99 or placebo. Immediately after this randomization and baseline assessments (lab tests and ECG), subjects will be given a 2-hour intra-venous infusion of DP-b99 or placebo. Additional 3 such infusions will then be given daily to a total of 4 consecutive treatment days, which make up the "Treatment Period". Throughout the 4-day Treatment Period the treatment's safety and the National Institutes of Health Stroke Scale (NIHSS) score will be evaluated daily. (The NIHSS assesses certain abilities of the patient, e.g. strength, speech, vision and coordination). If their condition requires, patients may have to stay in hospital more than these 4 days, regardless of their participation in the study.Subjects will be further assessed for NIHSS score changes and safety (lab tests and ECG) during the Post-treatment Follow-up Period, with data collected 30 and 90 days after the stroke. Other outcome scales (Barthel Index and Modified Rankin Scale) will be also used in the Day 30 and Day 90 visits

02

Conditions studied

  • Brain Ischemia
  • Stroke
  • Cerebrovascular Disorders

Keywords

  • Cerebral Ischemia
  • Ischemic Brain Injury
  • Brain Infarction
  • Brain Ischemia
03

In context

Stroke

7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.

This study's enrollment of 150 is above the median of 50 across 5,369 interventional studies indexed under Stroke.

Browse Stroke studies →

Lead sponsor

D-Pharm Ltd. is the lead sponsor of 6 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 85 Years
Sexes eligible
All
Accepts healthy volunteers
No

Eligibility criteria

Patients that may enter the study:

  • Patients with ischemic stroke, (that is, stroke that results from a blockage of blood flow to part of the brain), which is accompanied by language dysfunction (e.g. inability to understand speech), visual field defect or inattention to one side of the body or the space around the patient.
  • Patients in whom the study treatment can start no less than 1 and not more than 9 hours after the stroke's onset
  • Patients with moderate-severe degree of neurological deficit in the 9 hours after stroke onset (defined as NIHSS score of 7 to 20
  • Patients that can understand the requirements of the study and are willing to provide written informed consent (If the subject is incapacitated, informed consent will be sought from a legally acceptable representative.)

Patients that cannot participate:

  • Patients with a brain (intracerebral or subarachnoid) hemorrhage per screening computed tomography scan candidates for thrombolytic therapy for the current stroke patients having a mental impairment that renders them incapable to understand the study's requirements patients with other diseases that in the investigator's opinion may lead, independently of the current stroke, to further deterioration in the subject's neurological status during the trial period, or may confuse the evaluation of the present stroke
  • Patients likely to undergo a procedure involving cardiopulmonary bypass during the study period
  • Patients with medical conditions that may not enable them to complete the study (e.g life-threatening diseases,)
  • Patients whose condition improves already during the screening period
  • Patients who already have functional limitations before the present study (retrospective Modified Rankin Scale score of >3)
  • Patients who suffered a stroke within the past 90 days that seems to have been in the same brain region as the current acute stroke
  • Patients with severe hypertension (systolic BP >210 mm Hg or diastolic BP >120 mm Hg) or hypotension (systolic BP \<90 mm Hg), Patients with significant history of renal or liver disease(s) (serum creatinine of > 2.0 mg/dL; alanine aminotransferase, aspartate aminotransferase, or gamma-glutamyl transferase values of > threefold the upper normal limit)
  • Patients with a platelet count of \<100,000/mm3
  • Female patients of childbearing potential who are not using adequate and effective birth control measures or who are pregnant or lactating (the screening evaluation of female subjects of childbearing potential will include a serum pregnancy test.)
  • Patients who are users of addictive agents, or alcoholics
  • Patients who have received an investigational drug within the 90 days before the present stroke or such that are past recipients of DP-b99
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double
Enrollment
150 participants

Interventions

  • DrugDP-b99
06

What researchers measure

Primary outcomes

  1. Change in the National Institutes of Health Stroke Scale (NIHSS) score from baseline to Day 90

Secondary outcomes

  1. Safety and tolerability Neurological recovery and function

07

Study locations

22 sites
  • Neurologische Klink GmbH der Rhoen-Klinikum AG
    Bad Neustadt / Saale, 97616, Germany
  • Charité - Universitätsmedizin Berlin / Campus Charité Mitte, Klinik und Poliklinik für Neurologie
    Berlin, 10117, Germany
  • Universitätsklinik Essen Klinik und Poliklinik für Neurologie
    Essen, 45122, Germany
  • Neurologische Universitätsklinik Abteilung für Neurologie
    Freiburg, 79106, Germany
  • Klinik und Poliklinik für Neurologie Klinikum der Universität zu Köln
    Köln, 50931, Germany
  • Universitätsklinikum Leipzig Klinik und Poliklinik für Neurologie
    Leipzig, 04103, Germany
  • Otto-von-Guericke-Universität Magdeburg Medizinische Fakultät, Klinik für Neurologie
    Magdeburg, 39120, Germany
  • Johannes Gutenberg-Universität Mainz Neurologische Klinik
    Mainz, 55101, Germany
  • Klinikum 1 Minden Neurologische Klinik
    Minden, 32427, Germany
  • Städtisches Krankenhaus München-Harlaching Abteilung für Neurologie
    München-Harlaching, 81545, Germany
  • Neurologische Klinik und Poliklinik Technische Universität München Klinikum rechts der Isar
    München, 81675, Germany
  • Städtisches Krankenhaus München-Bogenhausen Abteilung für Neurologie und Klinische
    München, 81925, Germany
  • Universitätsklinikum Münster Klinik und Poliklinik für Neurologie
    Münster, 48129, Germany
  • Klinikum Osnabrück Abteilung Neurologie
    Osnabrück, 49076, Germany
  • Knappschaftskrankenhaus Recklinghausen Klinik für Neurologie und Klinische Neurophysiologie
    Recklinghausen, 45657, Germany
  • Universitätsklinikum Ulm Abteilung für Neurologie im RKU
    Ulm, 89081, Germany
  • Medizinisches Zentrum Kreis Aachen gGmbH Klinik für Neurologie
    Würselen-Bardenberg, 52146, Germany
  • Rambam Medical Center
    Haifa, 31096, Israel
  • Wolfson Medical Center
    Holon, 58220, Israel
  • Hadassah Ein Kerem Medical Center
    Jerusalem, 91120, Israel
  • Tel Aviv Sourasky Medical Center
    Tel Aviv, 64239, Israel
  • Chaim Sheba Medical Center
    Tel Hashomer, 52621, Israel
08

References and documents

Publications

  • Oral Session on Acute stroke: treatment concepts, presented on Thursday, 31 May 2007 at the XVI. European Stroke Conference, Glasgow, United Kingdom, 29 May - 1 June 2007. The abstract can be found at: http://www.esc-archive.eu/glasgow07/gla_so10_1.asp
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Nov 26, 2007, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT00190047
Lead sponsor
D-Pharm Ltd.
First posted
Sep 19, 2005
Start date
Feb 2005
Completion
Oct 2006
Last update
Nov 26, 2007

Study contacts

Gilad Rosenberg, M.D.
study director · D-Pharm Ltd.
View the source record on ClinicalTrials.gov ↗

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