Rosuvastatin

Generic Name
Rosuvastatin
Brand Names
Crestor, Ezallor, Roszet
Drug Type
Small Molecule
Chemical Formula
C22H28FN3O6S
CAS Number
287714-41-4
Unique Ingredient Identifier
413KH5ZJ73
Background

Rosuvastatin, also known as the brand name product Crestor, is a lipid-lowering drug that belongs to the statin class of medications, which are used to lower the risk of cardiovascular disease and manage elevated lipid levels by inhibiting the endogenous production of cholesterol in the liver. More specifically, statin medications competitively inhibit the enzyme hydroxymethylglutaryl-coenzyme A (HMG-CoA) Reductase, which catalyzes the conversion of HMG-CoA to mevalonic acid and is the third step in a sequence of metabolic reactions involved in the production of several compounds involved in lipid metabolism and transport including cholesterol, low-density lipoprotein (LDL) (sometimes referred to as "bad cholesterol"), and very low-density lipoprotein (VLDL). Prescribing of statin medications is considered standard practice following any cardiovascular events and for people with a moderate to high risk of development of CVD, such as those with Type 2 Diabetes. The clear evidence of the benefit of statin use coupled with very minimal side effects or long term effects has resulted in this class becoming one of the most widely prescribed medications in North America.

Rosuvastatin and other drugs from the statin class of medications including atorvastatin, pravastatin, simvastatin, fluvastatin, and lovastatin are considered first-line options for the treatment of dyslipidemia. This is largely due to the fact that cardiovascular disease (CVD), which includes heart attack, atherosclerosis, angina, peripheral artery disease, and stroke, has become a leading cause of death in high-income countries and a major cause of morbidity around the world. Elevated cholesterol levels, and in particular, elevated low-density lipoprotein (LDL) levels, are an important risk factor for the development of CVD. Use of statins to target and reduce LDL levels has been shown in a number of landmark studies to significantly reduce the risk of development of CVD and all-cause mortality. Statins are considered a cost-effective treatment option for CVD due to their evidence of reducing all-cause mortality including fatal and non-fatal CVD as well as the need for surgical revascularization or angioplasty following a heart attack. Evidence has shown that even for low-risk individuals (with <10% risk of a major vascular event occurring within 5 years) statins cause a 20%-22% relative reduction in major cardiovascular events (heart attack, stroke, coronary revascularization, and coronary death) for every 1 mmol/L reduction in LDL without any significant side effects or risks.

While all statin medications are considered equally effective from a clinical standpoint, rosuvastatin is considered the most potent; doses of 10 to 40mg rosuvastatin per day were found in clinical studies to result in a 45.8% to 54.6% decreases in LDL cholesterol levels, which is about three-fold more potent than atorvastatin's effects on LDL cholesterol. However, the results of the SATURN trial concluded that despite this difference in potency, there was no difference in their effect on the progression of coronary atherosclerosis.

Rosuvastatin is also a unique member of the class of statins due to its high hydrophilicity which increases hepatic uptake at the site of action, low bioavailability, and minimal metabolism via the Cytochrome P450 system. This last point results in less risk of drug-drug interactions compared to atorvastatin, lovastatin, and simvastatin, which are all extensively metabolized by Cytochrome P450 (CYP) 3A4, an enzyme involved in the metabolism of many commonly used drugs. Drugs such as ciclosporin, gemfibrozil, and some antiretrovirals are more likely to interact with this statin through antagonism of OATP1B1 organic anion transporter protein 1B1-mediated hepatic uptake of rosuvastatin.

Indication

The FDA monograph states that rosuvastatin is indicated as an adjunct to diet in the treatment of triglyceridemia, Primary Dysbetalipoproteinemia (Type III Hyperlipoproteinemia), and Homozygous Familial Hypercholesterolemia.

The Health Canada monograph for rosuvastatin further specifies that rosuvastatin is indicated for the reduction of elevated total cholesterol (Total-C), LDL-C, ApoB, the Total-C/HDL-C ratio and triglycerides (TG) and for increasing HDL-C in hyperlipidemic and dyslipidemic conditions when response to diet and exercise alone has been inadequate. It is also indicated for the prevention of major cardiovascular events (including risk of myocardial infarction, nonfatal stroke, and coronary artery revascularization) in adult patients without documented history of cardiovascular or cerebrovascular events, but with at least two conventional risk factors for cardiovascular disease.

Prescribing of statin medications is considered standard practice following any cardiovascular events and for people with a moderate to high risk of development of CVD. Statin-indicated conditions include diabetes mellitus, clinical atherosclerosis (including myocardial infarction, acute coronary syndromes, stable angina, documented coronary artery disease, stroke, trans ischemic attack (TIA), documented carotid disease, peripheral artery disease, and claudication), abdominal aortic aneurysm, chronic kidney disease, and severely elevated LDL-C levels.

Associated Conditions
Atherosclerosis, Atherosclerotic Cardiovascular Diseases, Cardiovascular Disease (CVD), Cardiovascular Events, Dysbetalipoproteinemia, Heterozygous Familial Hypercholesterolemia (HeFH), High Cholesterol, Homozygous Familial Hypercholesterolaemia (HoFH), Hypertension, Hypertension, Essential Hypertension, Hypertriglyceridemias, Major Adverse Cardiovascular Events, Mixed Dyslipidemias, Postoperative Thromboembolism, Primary Hypercholesterolemia, Primary Hyperlipidemia
Associated Therapies
Lipid-Lowering Therapy, Primary Prevention of Cardiovascular Diseases

Rosuvastatin Pre-Treatment Influences the Risk of Coronary Intervention Study

Phase 3
Conditions
Interventions
First Posted Date
2011-06-22
Last Posted Date
2011-06-22
Lead Sponsor
University Hospital, Motol
Target Recruit Count
400
Registration Number
NCT01378715
Locations
🇨🇿

Dpt. of Cardiology, Hospital Podlesi, Třinec, Czech Republic

🇨🇿

1st Medical Dept., Faculty of Medicine in Plzen, Charles University in Prague, University Hospital Plzen, Plzen, Czech Republic

🇸🇰

Eastern Slovakia Institute of Cardiovascular Diseases, Kosice, Slovakia

and more 1 locations

The Effects of Very Early Use of Rosuvastatin in Preventing Recurrence of Ischemic Stroke

Phase 3
Terminated
Conditions
Interventions
First Posted Date
2011-06-02
Last Posted Date
2014-11-20
Lead Sponsor
Severance Hospital
Target Recruit Count
318
Registration Number
NCT01364220
Locations
🇰🇷

Department of Neurology, Ewha Womans University Hospital, Seoul, Korea, Republic of

🇰🇷

Department of Neurology Colleage of Medicine Dong-A University, Busan, Korea, Republic of

🇰🇷

Department of Neurology, College of Medicine Inje University, Paik Hospital, Busan, Korea, Republic of

and more 24 locations

Rosuvastatin to Lower Circulating Tissue Factor Bearing Microparticles in Metastatic Breast Cancer

Phase 2
Completed
Conditions
Interventions
First Posted Date
2011-02-18
Last Posted Date
2020-02-05
Lead Sponsor
Beth Israel Deaconess Medical Center
Target Recruit Count
20
Registration Number
NCT01299038
Locations
🇺🇸

Dana-Farber Cancer Institute, Boston, Massachusetts, United States

🇺🇸

Beth Israel Deaconess Medical Center, Boston, Massachusetts, United States

Early Use of Rosuvastatin in Acute Coronary Syndromes: Targeting Platelet-Leukocyte Interactions

First Posted Date
2010-11-16
Last Posted Date
2017-03-28
Lead Sponsor
Susan Smyth
Target Recruit Count
54
Registration Number
NCT01241903
Locations
🇺🇸

University of Kentucky Dept of Cardiology, Lexington, Kentucky, United States

Influence of Organic Anion Transporting Polypeptide1B1(OATP1B1) Genotype on Rosuvastatin PK, PD and Lipid Profiles

First Posted Date
2010-10-11
Last Posted Date
2011-01-06
Lead Sponsor
Seoul National University Hospital
Target Recruit Count
34
Registration Number
NCT01218347
Locations
🇰🇷

Clinical Trials Center, Seoul National University Hospital, Seoul, Korea, Republic of

Effect of Intensive Lipid Lowering Treatment Compared to Moderate Lipid Lowering Treatment on Carotid Intima-media Thickness (CIMT)

First Posted Date
2010-09-17
Last Posted Date
2010-09-17
Lead Sponsor
Odense University Hospital
Target Recruit Count
87
Registration Number
NCT01203982
Locations
🇩🇰

Department of Cardiology, Odense University Hospital, Odense, Fuenen, Denmark

Statin Contrast Induced Nephropathy Prevention

Phase 4
Completed
Conditions
Interventions
First Posted Date
2010-08-20
Last Posted Date
2012-10-19
Lead Sponsor
Centro Cardiopatici Toscani
Target Recruit Count
500
Registration Number
NCT01185938
Locations
🇮🇹

Cardiology Division, Prato Hospital, Prato, Italy

Primary Prevention of Major Adverse Cardiac Events (MACE) With Standard and Intensive Statin Treatment in Patients With Diabetes: Survival and Cardiovascular Event Assessments

First Posted Date
2010-08-02
Last Posted Date
2011-06-01
Lead Sponsor
Positive Trial Group
Target Recruit Count
10000
Registration Number
NCT01173939
Locations
🇯🇵

Seiwadai Clinic, Kitakatsuragi gun, Nara pref., Japan

🇯🇵

Sato Clinic, Suzaka city, Nagano pref., Japan

🇯🇵

Abies Clinic, Fukuoka city, Fukuoka pref., Japan

and more 306 locations

A Trial of Rosuvastatin in Systemic Lupus Erythematosus

First Posted Date
2010-07-27
Last Posted Date
2015-06-23
Lead Sponsor
Imperial College London
Target Recruit Count
33
Registration Number
NCT01170585
Locations
🇬🇧

North West London Hospitals NHS Trust, London, United Kingdom

🇬🇧

Imperial College NHS Trust, London, United Kingdom

© Copyright 2024. All Rights Reserved by MedPath