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Terminated Phase 2 Interventional

Phase 2 Proof-of-Concept Study of the Safety and Efficacy of Alfimeprase to Rapidly Open Arteries and Restore Brain Function Following a Stroke

ClinicalTrials.gov ID: NCT00499902

Public ClinicalTrials.gov record NCT00499902. 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 Oct 24, 2026, 3:59 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

Phase 2, Multicenter, Open-Label, Two-Stage Study to Evaluate the Safety and Efficacy of Intra-Arterial Catheter-Directed Alfimeprase for Restoration of Neurologic Function and Rapid Opening of Arteries in Stroke (CARNEROS-1)

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to identify a safe and effective bolus dose of intra-arterial/intra-thrombus alfimeprase in acute ischemic stroke (AIS) 3 to 9 hours from symptom onset.

Study identification

NCT ID
NCT00499902
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 2
Lead sponsor
ARCA Biopharma, Inc.
Industry
Enrollment
7 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 85 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
Jun 2007 (Type not available)
Primary completion
May 2008 (Estimated)
Completion
May 2008 (Estimated)
Last update posted
Apr 24, 2008

2007 – 2008

United States locations

U.S. sites
17
U.S. states
12
U.S. cities
16
Facility City State ZIP Site status
UCLA Medical Center Los Angeles California 90024 —
Northwestern Medical Center Chicago Illinois 60611 —
Ruan Neurology & Clinical Research Center Des Moines Iowa 50314 —
University of Iowa Hospital Iowa City Iowa 52242 —
University of Iowa Hospital Iowa City Iowa 53342 —
University of Kansas School of Medicine, Via Christi Regional Medical Center Wichita Kansas 67214 —
Norton Hospital Louisville Kentucky 40202 —
Michigan State University, Sparrow Hospital Lansing Michigan 48912 —
Albany Medical Center Hospital Albany New York 12208 —
Kalieda Health, MFH Buffalo New York 14203 —
Columbia Presbyterian Medical Center New York New York 10032 —
University of Cincinnati Cincinnati Ohio 45243 —
Riverside Methodist Hospital Columbus Ohio 43214 —
Oregon Stroke Center Portland Oregon 97239 —
University of Pittsburg Medical Center Pittsburgh Pennsylvania 15213 —
Baylor College of Medicine Houston Texas 77030 —
St. Luke's Medical Center Milwaukee Wisconsin 53215 —

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00499902, 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 Apr 24, 2008 · Synced Oct 24, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00499902 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →