Epanova® for Lowering Very High Triglycerides

Completed · Phase 2/Phase 3 · Has a placebo group

Conditions studied: Severe Hypertriglyceridemia

In brief

The primary objective of the study is to determine the efficacy of Epanova (omefas) compared to placebo in lowering serum triglycerides in subjects with severe hypertriglyceridemia.

Key facts

Study ID

NCT01242527

Run by

AstraZeneca

People needed

399

Starts

2011-01-01

Expected to finish

2012-04-01

Last updated by the study team

2016-08-04

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Men or women, >=18 years of age.
• Very high serum TG values in the range >=500 mg/dL and <2000 mg/dL (>=5.65 mmol/L and <22.60 mmol/L)

You may not qualify if…

• Allergy or intolerance to omega-3 fatty acids, omega-3-acid ethyl esters, or fish.
• Known lipoprotein lipase impairment or deficiency or apolipoprotein C-II deficiency or familial dysbetalipoproteinemia.
• Unable to discontinue use of omega-3 drugs/supplements.
• Unable to discontinue use of bile acid sequestrants, fibrates or niacin (other than niacin-containing vitamins <200 mg), or any supplement used to alter lipid metabolism.
• Women who are pregnant, lactating, or planning to become pregnant. Women of childbearing potential who are not using acceptable contraceptive methods.
• Use of tamoxifen, estrogens or progestins that has not been stable for >4 weeks prior to Visit 1.
• Use of oral or injected corticosteroids or anabolic steroids.
• History of pancreatitis.
• History of symptomatic gallstone disease, unless treated with cholecystectomy.
• Uncontrolled diabetes.
• Uncontrolled hypothyroidism or thyroid stimulating hormone (TSH).
• History of cancer (other than basal cell carcinoma) in the past 2 years.
• Cardiovascular event (i.e., myocardial infarction, acute coronary syndrome, new onset angina, stroke, transient ischemic attack, unstable congestive heart failure requiring a change in treatment) or revascularization procedure within six months prior to Visit 1.
• Use of anticoagulants (e.g. warfarin [Coumadin®], coumarin, heparin, enoxaparin, clopidogrel).
• Presence of an aortic aneurysm or resection of an aortic aneurysm within six months prior to Visit 1.
• Recent history (within six months prior to Visit 1) or current significant nephrotic syndrome, pulmonary, hepatic, biliary, gastrointestinal or immunologic disease.
• Poorly controlled hypertension.
• Any of the following laboratory criteria: serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST), glucose, glomerular filtration rate (GFR), platelet count,or hemoglobin outside of study range.
• Recent history (past 12 months) of drug abuse or alcohol abuse.
• Exposure to any investigational product, within 4 weeks prior to Visit 1.
• Presence of any other condition the Investigator believes would interfere with the subject's ability to provide informed consent, comply with study instructions, or which might confound the interpretation of the study results or put the subject at undue risk

Where it is running

• Study site — Sacramento, California, United States
• Study site — Manchester, Connecticut, United States
• Study site — Coral Gables, Florida, United States
• Study site — Hialeah, Florida, United States
• Study site — Miami, Florida, United States
• Study site — Ocala, Florida, United States
• Study site — St. Petersburg, Florida, United States
• Study site — Summerfield, Florida, United States
• Study site — Atlanta, Georgia, United States
• Study site — Addison, Illinois, United States
• Study site — Chicago, Illinois, United States
• Study site — Louisville, Kentucky, United States
• Study site — Auburn, Maine, United States
• Study site — Olive Branch, Mississippi, United States
• Study site — High Point, North Carolina, United States
• Study site — Salisbury, North Carolina, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Cincinnati, Ohio, United States
• Study site — Columbus, Ohio, United States
• Study site — Oklahoma City, Oklahoma, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Philadelphia, Pennsylvania, United States
• Study site — Bristol, Tennessee, United States
• Study site — Johnson City, Tennessee, United States
• Study site — National City, California, United States

Full record on ClinicalTrials.gov

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