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Completed Phase 2 Interventional

Trial of VLTS-589 in Subjects With Intermittent Claudication

ClinicalTrials.gov ID: NCT00068133

Public ClinicalTrials.gov record NCT00068133. 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, 11:20 AM 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 Phase II Multicenter, Double-Blind, Placebo-Controlled, Trial of VLTS-589 in Subjects With Intermittent Claudication Secondary to Peripheral Arterial Disease

Study identification

NCT ID
NCT00068133
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Valentis
Industry
Enrollment
100 participants

Conditions and interventions

Interventions

  • Plasmid based Gene Transfer product-VLTS-589 Genetic

Genetic

Eligibility (public fields only)

Age range
40 Years to 80 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
May 31, 2003
Primary completion
Not listed
Completion
May 31, 2005
Last update posted
Jun 23, 2005

2003 – 2005

United States locations

U.S. sites
20
U.S. states
18
U.S. cities
20
Facility City State ZIP Site status
Cardiology Pc Birmingham Alabama 35211
Arizona Heart Institute Phoenix Arizona 85016
Access Clinical Trials-Cardiovascular Research Beverly Hills California 90210
Jacksonville Heart Center Jacksonville Florida 32207
Heart Specialists of Sarasota Clinical Research Center Sarasota Florida 34239
American Cardiovascular Research Institute Atlanta Georgia 30342
Rush Presbyterian St. Luke's Medical Center Chicago Illinois 60612
Prairie Heart Institution at St. John's Hospital Springfield Illinois 62701
The Care Group Indianapolis Indiana 46260
New Orleans Center for Clinical Research New Orleans Louisiana 70119
Androscoggin Cardiology Associates Auburn Maine 04210
University of Michigan Health Systems Ann Arbor Michigan 48109
Minneapolis Heart Institution Foundation Minneapolis Minnesota 55407
Dartmouth-Hitchcock Medical Center Lebanon New Hampshire 03756
St. Vincent's Hospital New York New York 10011
Duke Clinical Research Institute Durham North Carolina 27715
University of Oklahoma Health Science Center Oklahoma City Oklahoma 73104
Vanderbilt University Medical Center Nashville Tennessee 37232
The Methodist Hospital Houston Texas 77030
Daniel Gottleib, MD Seattle Washington 98166

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

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00068133, 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 23, 2005 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00068133 live on ClinicalTrials.gov.

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