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CompletedNCT00229177

Study of ONO-2506 in Patients With Acute Ischemic Stroke

Controlled Study of ONO-2506 in Patients With Acute Ischemic Stroke

Status
Completed
Phase
Phase 2 / Phase 3
Study type
Interventional
Enrollment
757 (actual)
Sponsor
Ono Pharmaceutical Co., Ltd. · Industry
Sex
All
Age
20 Years – 79 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the efficacy and safety of ONO-2506 compared to placebo in patients with acute ischemic stroke.

Conditions

Interventions

TypeNameDescription
DRUGONO-2506Once daily one-hour intravenous infusion at 12/mg/kg/hr for 7 days
DRUGONO-2506Once daily one-hour intravenous infusion at 0 mg/kg/hr for 7 days
DRUGONO-2506Once daily one-hour intravenous infusion at 8 mg/kg/hr for 7 days

Timeline

Start date
2005-09-01
Primary completion
2008-09-01
Completion
2008-09-01
First posted
2005-09-29
Last updated
2012-06-13

Locations

9 sites across 1 country: Japan

Source: ClinicalTrials.gov record NCT00229177. Inclusion in this directory is not an endorsement.

Study of ONO-2506 in Patients With Acute Ischemic Stroke (NCT00229177) · Clinical Trials Directory