MedPath

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

Esperion Secures Patent Protection for NEXLETOL Until 2040 Through Settlement with Micro Labs

• Esperion Therapeutics has reached a settlement agreement with Micro Labs that prevents the generic manufacturer from marketing a version of NEXLETOL (bempedoic acid) before April 19, 2040. • The agreement resolves patent litigation initiated by Esperion in response to Micro Labs' Abbreviated New Drug Application seeking approval for a generic version of the cholesterol-lowering medication. • Litigation against eight other ANDA filers continues, with no guarantee that these ongoing cases will prevent other generic versions from entering the market before the 2040 patent expiration.

Esperion Expands Global Reach: New Partnerships with CSL Seqirus and HLS Therapeutics for NEXLETOL and NEXLIZET

• Esperion Therapeutics has secured exclusive commercialization agreements with CSL Seqirus for Australia/New Zealand and HLS Therapeutics for Canada, expanding global access to its cholesterol-lowering medications NEXLETOL and NEXLIZET. • The partnerships include upfront payments and milestone-based compensation, with CSL Seqirus deal worth up to $5 million plus transfer pricing and HLS agreement including royalties on future Canadian sales. • Both medications are indicated to reduce cardiovascular risk and lower LDL-C in patients unable to take statins, addressing significant unmet needs in regions where cardiovascular disease affects millions.

Glenmark Pharmaceuticals Reaches $7M Settlement in US Antitrust Lawsuits Over Cholesterol Drugs

• Glenmark Pharmaceuticals has agreed to pay $7 million to settle antitrust lawsuits with three major healthcare entities - Humana, Centene, and Kaiser - over generic cholesterol medications Zetia and Vytorin. • The lawsuits alleged that Glenmark entered an anticompetitive agreement in 2010 with Schering Corporation and MSP Singapore Company LLC regarding patent infringement litigation for ezetimibe. • While reaching the settlement agreement, Glenmark explicitly denies all allegations and maintains the settlement does not indicate any admission of liability or illegal conduct.

Amneal Launches Generic Ezetimibe, Competing with $2.7B Zetia Market

• Amneal Pharmaceuticals has introduced generic ezetimibe tablets, a direct competitor to Merck's cholesterol-lowering drug Zetia, in 10mg strength across multiple bottle sizes. • The generic launch targets a substantial market opportunity, with Zetia recording approximately $2.7 billion in annual U.S. sales as of April 2017. • Distribution has commenced from Amneal's Kentucky facility, offering healthcare providers and patients a more affordable alternative to the branded medication.

Esperion Files for Canadian Approval of Nexletol and Nexlizet for LDL-C Reduction and Cardiovascular Risk

• Esperion has submitted New Drug Submissions (NDSs) in Canada for Nexletol and Nexlizet, seeking approval for LDL-C reduction and cardiovascular risk management. • Nexletol (bempedoic acid) and Nexlizet (bempedoic acid and ezetimibe) are oral, non-statin medications already approved in the United States and Europe. • Heart disease is a leading cause of death in Canada, affecting approximately 2.6 million adults, highlighting the need for new treatment options. • The submissions are based on data, including the CLEAR outcomes study, supporting the drugs' efficacy in reducing cardiovascular risk and LDL-C levels.

Esperion Therapeutics Reports Increased Revenue and Reduced Net Loss in Q3 2024

• Esperion Therapeutics reports a net product revenue increase of $10.8 million compared to Q3 2023, driven by prescription growth of NEXLETOL and NEXLIZET. • The company's R&D expenses decreased by $4.5 million due to the completion of the CLEAR Outcomes study, contributing to a reduced net loss of $29.5 million. • Esperion anticipates that current cash resources, expected future net product sales, and revenue under collaboration agreements will be sufficient to fund operations for the foreseeable future.
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