Overview

MK0767 in Metabolic Syndrome-Dyslipidemia (0767-016)

Status:
Terminated
Trial end date:
2003-12-01
Target enrollment:
0
Participant gender:
All
Summary
This is a clinical trial in patients with Metabolic Syndrome and Dyslipidemia to study the effects of MK0767 on triglycerides.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Merck Sharp & Dohme Corp.
Treatments:
Fenofibrate
Criteria
Inclusion Criteria:

- Patients with Metabolic Syndrome and Dyslipidemia age 21 to 65

- Patients will be eligible for the study if their triglyceride levels are within
protocol specified range and have at least 2 of the criteria for Metabolic Syndrome as
defined by NCEP

Exclusion Criteria:

- Patients with a history of diabetes mellitus, partial ileal bypass, intolerant to
fibric acid derivatives, requiring continuous oral corticosteroids, taking
anti-seizure medications, documented coronary heart disease, renal insufficiency,
proteinuria, viral hepatitis, cholelithiasis or other gallbladder disease,
pancreatitis, neoplastic disease

- Patient is on cyclical estrogen medications

- Patient has taken lipid-lowering agents including fibric acid derivatives, bile acid
sequestrants, HMG CoA reductase inhibitors and nicotinic acid derivatives within 8
weeks or probucol within 1 year of prior to visit 2