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Ezetimibe

Generic Name
Ezetimibe
Brand Names
Ezetrol, Lypqozet, Nexlizet, Roszet, Vytorin, Zetia
Drug Type
Small Molecule
Chemical Formula
C24H21F2NO3
CAS Number
163222-33-1
Unique Ingredient Identifier
EOR26LQQ24
Background

Ezetimibe is a lipid-lowering compound that inhibits intestinal cholesterol and phytosterol absorption. The discovery and research of this drug began in the early 1990s, after the intravenous administration of radiolabelled ezetimibe in rats revealed that it was being localized within enterocytes of the intestinal villi - this prompted studies investigating the effect of ezetimibe on intestinal cholesterol absorption. Ezetimibe is used as an adjunctive therapy to a healthy diet to lower cholesterol levels in primary hyperlipidemia, mixed hyperlipidemia, homozygous familial hypercholesterolemia (HoFH), and homozygous sitosterolemia (phytosterolemia).

Unlike other classes of cholesterol-reducing compounds including statins and bile acid sequestrants, ezetimibe has a distinct mechanism of action involving the sterol transporter Niemann-Pick C1-Like 1 (NPC1L1), and is unique in that it does not affect the absorption of fat-soluble nutrients such as fat-soluble vitamins, triglycerides, or bile acids. In genetically NPC1L1-deficient mice, a 70% reduction in intestinal cholesterol absorption was seen, and these mice were insensitive to ezetimibe treatment - it was determined based on these findings that NPC1L1 plays an essential role in promoting intestinal cholesterol uptake via an ezetimibe-sensitive pathway. By interfering with the intestinal uptake of cholesterol and phytosterols, ezetimibe reduces the delivery of intestinal cholesterol to the liver.

Indication

Ezetimibe is indicated to reduce elevated total-C, LDL-C, Apo B, and non-HDL-C in patients with primary hyperlipidemia, alone or in combination with an HMG-CoA reductase inhibitor (statin). It is also indicated to reduce elevated total-C, LDL-C, Apo B, and non-HDL-C in patients with mixed hyperlipidemia in combination with fenofibrate, and to reduce elevated total-C and LDL-C in patients with homozygous familial hypercholesterolemia (HoFH), in combination with atorvastatin or simvastatin. Ezetimibe may also be used to reduce elevated sitosterol and campesterol in patients with homozygous sitosterolemia (phytosterolemia).

Associated Conditions
Elevated Blood Lipids, Elevated sitosterol and campesterol
Associated Therapies
-

Ezetimibe and Simvastatin in Dyslipidemia of Diabetes

Phase 2
Completed
Conditions
Type 2 Diabetes
First Posted Date
2005-09-12
Last Posted Date
2007-02-13
Lead Sponsor
Mario Negri Institute for Pharmacological Research
Target Recruit Count
108
Registration Number
NCT00157482
Locations
🇮🇹

Hospital "Ospedali Riuniti di Bergamo" - Diabetologic Unit, Bergamo, Italy

🇮🇹

Hospital "Treviglio Caravaggio " - Diabetologic Unit, Treviglio, Bergamo, Italy

🇮🇹

Clinical Research Center for Rare Diseases, Ranica, Bergamo, Italy

and more 1 locations

A Study to Evaluate the Effects of Ezetimibe (MK-0653) on the Postprandial (Following a Meal) Lipoprotein Response in Participants With Primary Hypercholesterolemia (High Cholesterol) (MK-0653-072)(COMPLETED)

Phase 3
Completed
Conditions
Hypercholesterolemia
Interventions
First Posted Date
2005-01-11
Last Posted Date
2024-06-18
Lead Sponsor
Organon and Co
Target Recruit Count
58
Registration Number
NCT00101439

Higher-Dose Ezetimibe to Treat Homozygous Sitosterolemia

Phase 3
Completed
Conditions
Heart Diseases
Metabolism, Inborn Errors
First Posted Date
2004-12-22
Last Posted Date
2008-03-04
Lead Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
Target Recruit Count
3
Registration Number
NCT00099996
Locations
🇺🇸

National Heart, Lung and Blood Institute (NHLBI), Bethesda, Maryland, United States

Safety, Effectiveness, and Tolerability of Ezetimibe Combined With Statins for the Treatment of High Cholesterol in HIV Infected Adults

Not Applicable
Completed
Conditions
HIV Infections
First Posted Date
2004-12-20
Last Posted Date
2012-10-29
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Target Recruit Count
44
Registration Number
NCT00099684
Locations
🇺🇸

Rush-Presbyterian/St. Lukes (Chicago), Chicago, Illinois, United States

🇺🇸

UCLA School of Medicine, Los Angeles, California, United States

🇺🇸

University of Pennsylvania, Philadelphia, Philadelphia, Pennsylvania, United States

and more 39 locations

Comparative Efficacy Evaluation of Lipids When Treated With Niaspan & Statin or Other Lipid-Modifying Therapies-COMPELL

Phase 4
Completed
Conditions
Dyslipidemia
Coronary Heart Disease
Atherosclerosis
Stroke
Diabetes
First Posted Date
2004-03-12
Last Posted Date
2006-11-01
Lead Sponsor
Kos Pharmaceuticals
Target Recruit Count
300
Registration Number
NCT00079638
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