EASEGO Study: Doubling of Atorvastatin/Simvastatin or INEGY in Patients With Hypercholesterolemia and Coronary Artery Disease(CAD)
Information source: Merck
Information obtained from ClinicalTrials.gov on June 20, 2008
Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Atherosclerosis
Intervention: Mk0653A; ezetimibe (+) simvastatin / Duration of Treatment: 12 weeks (Drug)
Phase: Phase 4
Status: Completed
Sponsored by: Merck Official(s) and/or principal investigator(s):
Medical Monitor, Study Director, Affiliation: Merck
Summary
In patients with coronary artery disease and a LDL-C level between 2. 5 mmol/L and 5. 0 mmol/L
on a stable (> 4 weeks) statin starting dose (simvastatin 20 mg or atorvastatin 10 mg),
investigate what the LCL-C lowering efficacy is of doubling the statin dose (to 40 mg
simvastatin or 20 mg atorvastatin) versus a combination tablet of ezetimibe 10 mg plus
simvastatin 20 mg once daily for 12 weeks. It is postulated that more patients reach their
LDL-C treatment goal with the combination tablet compared to doubling the starting dose.
Furthermore, the effect of both treatment regimens on other lipid parameters, safety and
LDL-subfractions will be measured.
Clinical Details
Official title: A Prospective Randomized Open Label Blinded Endpoint Multicenter Study in Patients With Coronary Artery Disease to Assess the LDL Lowering Effect of Switching to Ezetimibe (+) Simvastatin for Cholesterol Lowering, Compared the Dose of the Statin Used.
Study design: Treatment, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Primary outcome: Switching to a combination tablet of ezetimibe 10 mg plus simvastatin 20 mg is superior to doubling the statin dose as demonstrated by the percentage of patients reaching goal after 12 weeks of treatment.
Secondary outcome: Switching to a combination tablet of ezetimibe 10 mg plus simvastatin 20 mg will lower LDL-C more than doubling the statin dose as demonstrated by the percentage change from treated baseline in total and LDL-cholesterol after 12 weeks of treatment.
Eligibility
Minimum age: 18 Years.
Maximum age: N/A.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Patient is male or female 18 years of age.
- Patient is on a stable daily statin starting dose for the past 4 weeks of either:
atorvastatin 10 mg or; simvastatin 20 mg
- lipid values while on statin monotherapy treatment: LDL-C level of > 2. 5 mmol/L to *
5. 0 mmol/L, triglycerides < 4. 0 mmol/L and total cholesterol < 7. 0 mmol/L.
- Patient with established coronary artery disease such as stable angina; history of
myocardial infarction; history of percutaneous coronary intervention (PTCA with or
without stent placement); coronary stenosis on angiography; history of unstable angina
or non-Q wave myocardial infarction; history of coronary artery bypass graft surgery
(CABG); positive MIBI scan. Patients have to be in a stable medical condition.
Exclusion Criteria:
- Patients in whom cholesterol lowering medication regime has changed in the previous 4
weeks.
- Patients who have been treated with any other investigational drug within 3 months of
Visit 1.
- Patients who are pregnant or lactating.
- Any condition or situation which, in the opinion of the investigator, might pose a
risk to the patient or interfere with participation in the study.
Locations and Contacts
Additional Information
Starting date: November 2005
Last updated: May 5, 2008
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