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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

Study of Ezetimibe and Fenofibrate in Patients With Mixed Hyperlipidemia (0653-036)(COMPLETED)

Phase 3
Completed
Conditions
Hypercholesterolemia
Hypertriglyceridemia
First Posted Date
2004-09-28
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
576
Registration Number
NCT00092573

Sitosterolemia Extension Study (0653-004)(COMPLETED)

Phase 3
Completed
Conditions
Heart Disease
Lipid Metabolism, Inborn Errors
First Posted Date
2004-09-28
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
58
Registration Number
NCT00092820

An Investigational Drug Study to Lower Non-Cholesterol Sterol Levels Associated With Sitosterolemia (0653-062)(COMPLETED)

Phase 3
Completed
Conditions
Lipid Metabolism, Inborn Errors
Heart Disease
First Posted Date
2004-09-28
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
30
Registration Number
NCT00092898

MK0653A (Ezetimibe (+) Simvastatin) Compared to an Approved Drug (Atorvastatin) for the Treatment of High Cholesterol (0653A-051)(COMPLETED)

Phase 3
Completed
Conditions
Hypercholesterolemia
First Posted Date
2004-09-28
Last Posted Date
2024-05-10
Lead Sponsor
Organon and Co
Target Recruit Count
1902
Registration Number
NCT00092690

Study of an Approved Drug With a Statin (a Medication That Lowers Cholesterol Levels) as Compared to Statin Therapy Alone in Patients With High Cholesterol (0653-040)

Phase 3
Completed
Conditions
Hypercholesterolemia
First Posted Date
2004-09-28
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
2904
Registration Number
NCT00092586

Investigational Drug Study in Patients With Elevated Cholesterol and Coronary Heart Disease (0653-801)

Phase 3
Completed
Conditions
Coronary Disease
Hypercholesterolemia
First Posted Date
2004-09-27
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
410
Registration Number
NCT00092599

An Investigational Drug Study in Patients With Elevated Cholesterol and Coronary Heart Disease (0653-804)(COMPLETED)

Phase 3
Completed
Conditions
Hypercholesterolemia
Coronary Disease
First Posted Date
2004-09-27
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
450
Registration Number
NCT00092638

Co-administration Study in Patients With Elevated Cholesterol and Coronary Heart Disease (0653-802)(COMPLETED)

Phase 3
Completed
Conditions
Hypercholesterolemia
Coronary Disease
First Posted Date
2004-09-27
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
372
Registration Number
NCT00092612

Co-administration Study in Patients With Elevated Cholesterol and Coronary Heart Disease (0653-803)

Phase 3
Completed
Conditions
Hypercholesterolemia
Coronary Disease
First Posted Date
2004-09-27
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
442
Registration Number
NCT00092625

Study to Evaluate the Cholesterol Lowering Effects of Two Marketed Drugs in Patients With Elevated Cholesterol Levels (0653A-058)

Phase 3
Completed
Conditions
Hypercholesterolemia
First Posted Date
2004-08-30
Last Posted Date
2024-08-15
Lead Sponsor
Organon and Co
Target Recruit Count
2815
Registration Number
NCT00090298
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