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

Stopped early · Phase 3 · Has a placebo group

Conditions studied: Stroke, Cerebral Ischemia, Brain Infarction

In brief

The primary purpose of this study is to determine whether a brief intravenous infusion of ancrod started within 6 hours of stroke onset improves functional outcome at 3 months.

Key facts

Study ID
NCT00141011
Run by
Neurobiological Technologies
People needed
277
Starts
2005-09-01
Expected to finish
2008-12-01
Last updated by the study team
2009-12-23

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

You may not qualify if…

Where it is running

Full record on ClinicalTrials.gov

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