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

Effects of Rosuvastatin on Aortic Stenosis Progression

Phase 3
Completed
Conditions
Interventions
First Posted Date
2008-12-02
Last Posted Date
2010-12-03
Lead Sponsor
AstraZeneca
Target Recruit Count
378
Registration Number
NCT00800800
Locations
🇨🇦

Research site, St. John's, Canada

Rosuvastatin Prevent Contrast Induced Acute Kidney Injury in Patients With Diabetes

Phase 4
Completed
Conditions
Interventions
First Posted Date
2008-11-06
Last Posted Date
2013-04-10
Lead Sponsor
Shenyang Northern Hospital
Target Recruit Count
2998
Registration Number
NCT00786136
Locations
🇨🇳

Renmin Hospital Of Wuhan University, WuHan, Hubei, China

🇨🇳

ShenZhou Hopital Of ShenYang Medical College, ShengYang, Liaoning, China

🇨🇳

WuHan Asia Heart Hosital, WuHan, Hubei, China

and more 50 locations

Exploratory Study of Coronary Flow Reserve Measurements, a Non-Invasive Method for Coronary Function Measurements

First Posted Date
2008-10-31
Last Posted Date
2009-06-30
Lead Sponsor
AstraZeneca
Target Recruit Count
80
Registration Number
NCT00783042
Locations
🇸🇪

Research Site, Goteborg, Sweden

A Diabetes Study to Treat A Population Previously Not at Target

Phase 4
Completed
Conditions
Interventions
First Posted Date
2008-09-04
Last Posted Date
2011-08-31
Lead Sponsor
AstraZeneca
Target Recruit Count
598
Registration Number
NCT00747149
Locations
🇨🇦

Research Site, Quebec, Canada

Effects of Crestor on Inflammation of Atherosclerotic Plaques

First Posted Date
2008-06-03
Last Posted Date
2009-06-30
Lead Sponsor
AstraZeneca
Target Recruit Count
74
Registration Number
NCT00689416
Locations
🇸🇪

Research Site, Uppsala, Sweden

Compare the Efficacy of Rosuvastatin to Atorvastatin in High Risk Patients With Hypercholesterolemia

Phase 3
Completed
Conditions
Interventions
First Posted Date
2008-05-23
Last Posted Date
2012-03-21
Lead Sponsor
AstraZeneca
Target Recruit Count
934
Registration Number
NCT00683618
Locations
🇨🇳

Research Site, Tianjin, China

Study to Compare the Bioavailability of ABT-335 and Rosuvastatin From ABT-143 Relative to That From the Co-administration of ABT-335 and Rosuvastatin Calcium

First Posted Date
2008-05-21
Last Posted Date
2012-09-28
Lead Sponsor
AstraZeneca
Target Recruit Count
64
Registration Number
NCT00681395
Locations
🇺🇸

Site Reference ID/Investigator# 8089, Orlando, Florida, United States

Rosuvastatin in Rheumatoid Arthritis (RORA)

Phase 2
Completed
Conditions
Interventions
First Posted Date
2008-05-19
Last Posted Date
2019-11-05
Lead Sponsor
University of Dundee
Target Recruit Count
50
Registration Number
NCT00679510
Locations
🇬🇧

University of Dundee, Dundee, United Kingdom

30 Week Study of the Combination of ABT-335 and Rosuvastatin Compared to Rosuvastatin Monotherapy for Subjects With Dyslipidemia and Stage 3 Chronic Kidney Disease

First Posted Date
2008-05-19
Last Posted Date
2012-10-03
Lead Sponsor
AstraZeneca
Target Recruit Count
280
Registration Number
NCT00680017
Locations
🇺🇸

Site Reference ID/Investigator# 8095, Philadelphia, Pennsylvania, United States

🇺🇸

Site Reference ID/Investigator# 22812, Dallas, Texas, United States

🇺🇸

Site Reference ID/Investigator# 8136, Atlanta, Georgia, United States

and more 111 locations

Effectiveness of Rosuvastatin at Preventing the Progression of Atherosclerosis in HIV Positive Patients

Phase 4
Terminated
Conditions
Interventions
First Posted Date
2008-05-07
Last Posted Date
2009-08-25
Lead Sponsor
University of British Columbia
Target Recruit Count
250
Registration Number
NCT00673582
Locations
🇨🇦

The St. Paul's Hospital HIV Metabolic Clinic & The BC Centre for Excellence in HIV/AIDS, Vancouver, British Columbia, Canada

© Copyright 2024. All Rights Reserved by MedPath