Tricor (fenofibrate) is a medication that has been licensed to treat several conditions. Tricor uses include the reduction of: Cholesterol levels in patients with hypercholesterolemia (high cholesterol). Tricor can reduce both total and LDL cholesterol (bad cholesterol) and raise HDL cholesterol (good cholesterol). Triglyceride levels in patients with hypertriglyceridemia (high triglycerides). Triglycerides are fat-like substances found in the body. TriCor contains the active ingredient fenofibrate and is available in tablet form. It is a lipid controling agent. Each tablet contains 40 mg or 120 mg fenofibrate. The inactive ingredients of TriCor contain lactose monohydrate, NF; Polyethylene Glycol 6000, NF; Poloxamer 188, NF; and magnesium stearate, NF. TriCor or fenofibrate is indicated as adjunctive therapy to diet to decrease increased LDL-C, Total-C, Triglycerides, and Apo B, and to increase HDL-C in adult patients with primary hyperlipidemia or mixed dyslipidemia. Lipid-altering medicaion should always be administered in conjunction with strict dietary protocol in saturated fat and cholesterol when the response to diet and non-pharmacological interventions is not working sufficiently.

Fenofibrate is a drug of the fibrate class. It is mainly used to reduce cholesterol levels in patients at risk of cardiovascular disease. Like other fibrates it reduces both low-density lipoprotein (LDL) and very low density lipoprotein (VLDL) levels, as well as increasing high-density liporotein (HDL) levels. It also appears to have a beneficial effect on the insulin resistance featured by the metabolic syndrome. It is used alone or in conjunction with statins in the treatment of hypercholesterolemia and hypertriglyceridemia. Fenofibrate is sold under the brand name Triglide by Sciele Pharma and Antara by Oscient Pharmaceuticals.

The pharmaceutical form and the strength may change from one country from another, and from one brand to another. In the United States, Ttricor was reformulated in 2005 and is available in tablets of 45 and 145 mg. This reformulation is controversial and is the subject of antitrust litigation by generic drug manufacturer Teva. In Europe, it is available in coated tablet but also in capsule, the strength range include 67, 145, 160 and 200 mg. The differences in strength belong is due to altered bioavailability (the fraction absorbed by the body) due to particle size. For example: 200 mg can be replaced by 160 mg because its fenofibrate is micronised. The 145 mg strength is a new strength appeared in 2005-2006 which also replaces 200 or 160 mg as the fenofibrate is nanonised (ie the particle size is below 400 nm). Antara is sold in the U.S. as capsules of 43 and 130 mg.

Like the other fibrates, fenofibrate acts on PPAR\u03B1 to reduce cholesterol levels.

A large study in 2005 of fenofibrate in patients with diabetes showed no change in total mortality or coronary artery events, but did show a significant change in overall cardiovascular events, as well as improving some microvascular complications of diabetes.

Like most fibrates, fenofibrate can cause stomach upsets and myopathy (muscle pain) and very rarely rhabdomyolysis. This risk is increased when used together with statins. However, the Fenofibrate Intervention and Event Lowering in Diabetes (FIELD) study provides important information that long-term treatment with fenofibrate therapy appears to have a favorable safety profile in patients with type 2 diabetes, even when nonstudy lipid-lowering medications were added. In FIELD, there were no cases of rhabdomyolysis reported in patients on combination therapy with fenofibrate and a statin. Thus, there is an increasing body of evidence that fenofibrate/statin combination therapy is safe and effective at managing dyslipidemia in patients with type 2 diabetes who are at risk for cardiovascular events.