Overview
MK0767 in Metabolic Syndrome-Dyslipidemia (0767-016)
Status:
Terminated
Terminated
Trial end date:
2003-12-01
2003-12-01
Target enrollment:
0
0
Participant gender:
All
All
Summary
This is a clinical trial in patients with Metabolic Syndrome and Dyslipidemia to study the effects of MK0767 on triglycerides.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
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