Viewing Study NCT00068133



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Last Modification Date: 2024-10-26 @ 9:09 AM
Study NCT ID: NCT00068133
Status: COMPLETED
Last Update Posted: 2005-06-24
First Post: 2003-09-08

Brief Title: Trial of VLTS-589 in Subjects With Intermittent Claudication
Sponsor: Valentis
Organization: Valentis

Study Overview

Official Title: A Phase II Multicenter Double-Blind Placebo-Controlled Trial of VLTS-589 in Subjects With Intermittent Claudication Secondary to Peripheral Arterial Disease
Status: COMPLETED
Status Verified Date: 2005-05
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The purpose of this study is to evaluate the safety and tolerability of VLTS-589 compared with placebo administered bilaterally to the lower extremities in subjects with intermittent claudication and to determine the effect of VLTS-589 in peak walking time PWT for subjects receiving VLTS-589 compared with subjects receiving placebo
Detailed Description: None

Study Oversight

Has Oversight DMC: None
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: None