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Efficacy and Safety of HMR1766 in Patients With Fontaine Stage II Peripheral Arterial Disease — ACCELA  

Intermittent Claudication Clinical Trial

Official title:
A Randomized, Double-blind, Placebo-controlled, Parallel Group Trial of HMR1766 Assessing the Efficacy and Safety of 3 Doses of HMR1766 Versus Placebo With Cilostazol as a Calibrator, Administered for 26 Weeks in Patients With Peripheral Arterial Disease (PAD) Fontaine Stage II

Clinical Trial Summary

The primary objective is to investigate in patients suffering from intermittent claudication due to Fontaine stage II Peripheral Arterial Disease (PAD) whether a 26-week treatment by HMR1766 on top of clopidogrel may result in an improvement of walking capacity, by comparing three doses of HMR1766 to placebo, and calibrating such effect versus cilostazol.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00443287
Study type Interventional
Source Sanofi
Contact
Status Completed
Phase Phase 2
Start date February 2007
Completion date October 2008
View Details
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