Clinical trial

Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke

NCT00141011 · Neurobiological Technologies, Industry · Terminated

Key facts

NCT number NCT00141011
Title Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke
Official title ASP I (Ancrod Stroke Program) Study of Acute Viprinex™ for Emergency Stroke: A Randomized, Double-Blind, Placebo-Controlled Study of Ancrod (Viprinex™) in Subjects Beginning Treatment Within 6 Hours of the Onset of Acute, Ischemic Stroke
Lead sponsor Neurobiological Technologies, Industry
Status Terminated
Phase Phase 3
Study type Interventional
Conditions Stroke, Cerebral Ischemia, Brain Infarction
Intervention type Drug
Interventions Ancrod (Viprinex), Placebo
Enrollment 277
Start date Sep 1, 2005
Primary completion Dec 1, 2008
Completion Dec 1, 2008
First posted Sep 1, 2005
Last update posted Dec 23, 2009
Countries Australia, Canada, Czechia, Netherlands, Poland, Russia, South Africa, Taiwan, United Kingdom, United States

At a glance

  • 100–999 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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