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Terminated Phase 2 Interventional

A Study to Evaluate the Efficacy and Safety of CP-101,606 in Subjects With an Acute Stroke

ClinicalTrials.gov ID: NCT00073476

Public ClinicalTrials.gov record NCT00073476. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 21, 2026, 5:28 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Placebo-Controlled, Multi-Center Study to Evaluate the Efficacy and Safety of a 72-Hour Infusion of CP-101,606 in Subjects With Acute Ischemic Stroke.

Study identification

NCT ID
NCT00073476
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
Pfizer
Industry
Enrollment
300 participants

Conditions and interventions

Conditions

Interventions

  • traxiprodil (CP-101,606) Drug

Drug

Eligibility (public fields only)

Age range
40 Years to 90 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Aug 31, 2003
Primary completion
Not listed
Completion
Jan 31, 2005
Last update posted
Jun 21, 2006

2003 – 2005

United States locations

U.S. sites
12
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
Pfizer Investigational Site La Mesa California 91942
Pfizer Investigational Site Atlanta Georgia 30342
Pfizer Investigational Site Fort Wayne Indiana 46804
Pfizer Investigational Site Fort Wayne Indiana 46805
Pfizer Investigational Site Louisville Kentucky 40202
Pfizer Investigational Site Salisbury North Carolina 28144
Pfizer Investigational Site Dayton Ohio 45406
Pfizer Investigational Site Dayton Ohio 45408
Pfizer Investigational Site Dayton Ohio 45409
Pfizer Investigational Site Dayton Ohio 45415
Pfizer Investigational Site Allentown Pennsylvania 18103
Pfizer Investigational Site Philadelphia Pennsylvania 19141

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 17 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00073476, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 21, 2006 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00073476 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →