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NCT00115999 · ClinicalTrials.gov registry record · Phase 3

Study of Alfimeprase to Rapidly Dissolve Blood Clots in the Leg and Help Prevent the Need for Surgery on Leg Arteries

A Phase 3 study of Arterial Occlusive Diseases, sponsored by ARCA Biopharma.

Completed
Registry status
Phase 3
Development phase
300
Enrollment target
1
Study location

NCT00115999 is a Phase 3 study of Arterial Occlusive Diseases that has completed, run by ARCA Biopharma. The registered enrollment target is 300 participants, roughly in line with the 283-participant average among 4 other Arterial Occlusive Diseases trials with a reported enrollment target. The trial reports 1 study location across 1 state.

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The verdict

NCT00115999, a Phase 3 study of Arterial Occlusive Diseases, has completed, sponsored by ARCA Biopharma.

COMPLETED
Registry status
Phase 3
Development phase
300 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to directly compare the safety and efficacy of intra-thrombus alfimeprase 0.3 mg/kg with placebo in acute peripheral arterial occlusion (PAO) as measured by a 30 day open vascular free surgery rate.

Interventions

  • DRUG alfimeprase

Study Locations (1)

Ohio

  • The Cleveland Clinic Foundation - Cleveland

Trial Details

FieldValue
Enrollment Target 300 participants
Start Date 2005-04
Est. Completion 2007-02
Phase Phase 3

Sponsor

ARCA Biopharma

10 total trials

What the Registry Record Tells You About NCT00115999

The ClinicalTrials.gov registry entry for NCT00115999 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 300 participants, a figure that helps gauge the scale of data the investigators plan to collect, roughly in line with the 283-participant average among 4 other Arterial Occlusive Diseases trials with a reported enrollment target. The listed sponsor is ARCA Biopharma, which has 10 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Arterial Occlusive Diseases appearing as the primary indexed condition, and to 1 intervention - of which alfimeprase is the first listed.

NCT00115999 reports 1 study location spanning 1 distinct geographic area - top geographies include Ohio.

Frequently Asked Questions

What is clinical trial NCT00115999 about?

NCT00115999 is a clinical study titled "Study of Alfimeprase to Rapidly Dissolve Blood Clots in the Leg and Help Prevent the Need for Surgery on Leg Arteries". The purpose of this study is to directly compare the safety and efficacy of intra-thrombus alfimeprase 0.3 mg/kg with placebo in acute peripheral arterial occlusion (PAO) as measured by a 30 day open vascular free surgery rate.

What is the current status of trial NCT00115999?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 300 participants. The study started on 2005-04. Estimated completion is 2007-02.

What conditions does trial NCT00115999 study?

This clinical trial studies the following conditions: Arterial Occlusive Diseases.

What interventions are being tested in trial NCT00115999?

The interventions under investigation include: alfimeprase (DRUG).

Who is sponsoring clinical trial NCT00115999?

This trial is sponsored by ARCA Biopharma, which has 10 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT00115999 being conducted?

This trial has 1 study location across Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

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