Overview

A Study of How MK-0736 Affects Arterial Plaque (0736-006)(TERMINATED)

Status:
Terminated
Trial end date:
2008-08-26
Target enrollment:
0
Participant gender:
All
Summary
A 12-Week Efficacy Study in participants with Peripheral Arterial Disease. the primary hypothesis is that MK-0736 7 mg administered once daily for 12 weeks will result in a decrease in lower extremity atherosclerotic plaque macrophage content when compared to placebo (an approximate decrease of up to 30% is expected).
Phase:
Phase 1
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Merck Sharp & Dohme Corp.
Collaborator:
FoxHollow Technologies
Criteria
Inclusion Criteria:

- Participants with peripheral arterial disease

- Participants must be 18 to 85 years of age

- Females must be postmenopausal or sterile

Exclusion Criteria:

- Participans with hepatic, HIV, endocrine, connective tissue, psychiatric disorders or
uncontrolled hypertension