EUCTR2004-003807-19-GB
Active, not recruiting
Phase 1
A Study to Evaluate the Efficacy and Safety of Ezetimibe/Simvastatin and Fenofibrate Coadministration in Patients With Mixed Hyperlipidemia - Ezetimibe/Simvastatin and Fenofibrate Coadministration Study
Merck Sharp & Dohme Ltd0 sites600 target enrollmentFebruary 24, 2005
DrugsSUPRALIP
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Mixed hyperlipidemia
- Sponsor
- Merck Sharp & Dohme Ltd
- Enrollment
- 600
- Status
- Active, not recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •a.Patient has an LDL\-C 130 through 220 mg/dL (3\.37 through 5\.70 mmol/L) for non\-diabetics; LDL\-C 100 through 180 mg/dL (2\.59 through 4\.66 mmol/L) for diabetics, at Visit 2\.
- •b.Patient has triglycerides 150 through 500 mg/dL (1\.71 through 5\.70 mmol/L). \[per central laboratory reference ranges] at Visit 2\.
- •c.Patient has creatine phosphokinase (CPK) \=2 x upper limit of normal (ULN) \[per central laboratory reference ranges] at Visit 2\.
- •d.Patient has alanine aminotransferase (ALT), and aspartate aminotransferase (AST) \=1\.5 x upper limit of normal (ULN) \[per central laboratory reference ranges] at Visit 2\.
- •Are the trial subjects under 18?
- •Number of subjects for this age range:
- •F.1\.2 Adults (18\-64 years) yes
- •F.1\.2\.1 Number of subjects for this age range
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range
Exclusion Criteria
- •a.You are less than 18 years of age or greater than 79 years of age.
- •b.You are pregnant, breastfeeding, or planning to become pregnant during this study.
- •c.You are a woman able to become pregnant and are not willing to use an acceptable method of birth control. You must be willing to use this birth control starting at Visit 1 and continuing 14 days past the last study dose. The study doctor or staff will discuss which methods of birth control are acceptable for this study.
- •d.You are a woman and have taken cyclical hormone birth control or hormone replacement within 8 weeks of Visit 3\.
- •e.You have chronic heart failure, uncontrolled irregular heart beats or a history of heart disease. The study doctor or staff will discuss this with you.
- •f.You have diabetes and are taking lipid lowering medication called statins.
- •g.You have a history of cholelithiasis (gallbladder problems) and you have not had your gallbladder removed.
- •h.You have an active liver disease.
- •i.You are HIV positive.
- •j.You have a history of cancer with in the past 5 years (except for skin cancer that has been successfully treated).
Outcomes
Primary Outcomes
Not specified
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