Overview
A Study to Evaluate the Efficacy and Safety of CP-101,606 in Subjects With an Acute Stroke
Status:
Terminated
Terminated
Trial end date:
2005-02-01
2005-02-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
The purpose of this study is to determine whether a new research medication is effective and safe for the treatment of acute stroke when given within 6 hours of the onset of stroke.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Pfizer
Criteria
Inclusion Criteria:Males & females age 40-90 years
Enrolled in study within 6 hours of onset of stroke symptoms
Willing to sign informed consent form
No significant disabilities prior to stroke
Exclusion Criteria:
Treatment with t-PA (tissue plasminogen activator)
Premorbid modified rankin scale score of 2 or more