drugset / Trial / NCT00300196

ASP-II: Ancrod Stroke Program: Ancrod (Viprinex™) for the Treatment of Acute, Ischemic Stroke

NCT00300196 ↗

Phase 3 Terminated 311 enrolled Neurobiological Technologies
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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.

Timeline

Start
2006-03
Primary completion
2008-12
Completion
2008-12

Outcome

Outcome not reported

Stopped: “Futility”

Drugs

EvaluationDrugModalityDoseRoute
Subject Ancrod Unknown 0.167 iu/kg Intravenous