A Study of AMR101 to Evaluate Its Ability to Reduce Cardiovascular Events in High Risk Patients With Hypertriglyceridemia and on Statin. The Primary Objective is to Evaluate the Effect of 4 g/Day AMR101 for Preventing the Occurrence of a First Major Cardiovascular Event.
Status: | Completed |
---|---|
Conditions: | Peripheral Vascular Disease, Metabolic |
Therapuetic Areas: | Cardiology / Vascular Diseases, Pharmacology / Toxicology |
Healthy: | No |
Age Range: | 45 - Any |
Updated: | 10/18/2018 |
Start Date: | November 2011 |
End Date: | May 2018 |
Evaluation of the Effect of AMR101 on Cardiovascular Health and Mortality in Hypertriglyceridemic Patients With Cardiovascular Disease or at High Risk for Cardiovascular Disease: REDUCE-IT (Reduction of Cardiovascular Events With EPA - Intervention Trial)
AMR101 (icosapent ethyl [ethyl-EPA]) is a highly purified ethyl ester of eicosapentaenoic
acid (EPA) being developed by Amarin Pharma Inc. for the treatment of cardiovascular disease
in statin-treated patients with hypertriglyceridemia. The purpose of this study is to
evaluate whether this drug, combined with a statin therapy, will be superior to the statin
therapy alone, when used as a prevention in reducing long-term cardiovascular events in
high-risk patients with mixed dyslipidemia.
acid (EPA) being developed by Amarin Pharma Inc. for the treatment of cardiovascular disease
in statin-treated patients with hypertriglyceridemia. The purpose of this study is to
evaluate whether this drug, combined with a statin therapy, will be superior to the statin
therapy alone, when used as a prevention in reducing long-term cardiovascular events in
high-risk patients with mixed dyslipidemia.
Inclusion Criteria:
- Men and non-pregnant or sterile women ages 45 and older
- Hypertriglyceridemia
- On statin therapy for at least four weeks
- Either having established Cardiovascular Disease or at high risk for Cardiovascular
Disease
Exclusion Criteria:
- Severe heart failure
- Any life-threatening disease other than Cardiovascular Disease
- Active severe liver disease
- Hemoglobin A1c >10.0%
- Poorly controlled hypertension
- Planned coronary intervention (such as stent placement or heart bypass) or any
non-cardiac major surgical procedure
- Known familial lipoprotein lipase deficiency (Fredrickson Type I), apolipoprotein C-II
deficiency, or familial dysbetalipoproteinemia (Fredrickson Type III)
- Known hypersensitivity to the study product, fish and/or shellfish, or placebo
- History of acute or chronic pancreatitis
- Patients are excluded if using the following medications:
- PCSK9 inhibitors
- niacin >200 mg/day or fibrates;
- any omega-3 fatty acid medications ;
- dietary supplements containing omega-3 fatty acids (e.g., flaxseed oil, fish oil,
krill oil, or algal oil);
- bile acid sequestrants
We found this trial at
177
sites
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