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

Pharmacodynamic Comparison of Rosuvastatin Versus Atorvastatin on Platelet Reactivity in Patients With Coronary Artery Disease on Dual Antiplatelet Therapy With New P2Y12 Inhibitors (Trial gRANADa)

First Posted Date
2014-01-08
Last Posted Date
2014-12-04
Lead Sponsor
University of Roma La Sapienza
Target Recruit Count
150
Registration Number
NCT02030054
Locations
🇮🇹

Sapienza Univeristy of Rome, Rome, Italy

Comparison of PK After Administration of HCP1201 and Co-administration of Metformin SR 750mg and Rosuvastatin 10mg

First Posted Date
2014-01-03
Last Posted Date
2014-03-11
Lead Sponsor
Hanmi Pharmaceutical Company Limited
Target Recruit Count
36
Registration Number
NCT02026817
Locations
🇰🇷

Samsung Medical Center, Seoul, Korea, Republic of

Comparison of PK After Administration of HCP1201 and Co-administration of Metformin SR 500mg and Rosuvastatin 10mg

First Posted Date
2013-12-13
Last Posted Date
2014-03-11
Lead Sponsor
Hanmi Pharmaceutical Company Limited
Target Recruit Count
72
Registration Number
NCT02011633
Locations
🇰🇷

Samsung Medical Center, Seoul, Korea, Republic of

Statin and Angiotensin-converting Enzyme Inhibitor on Symptoms in Patients With SCAD

First Posted Date
2013-12-11
Last Posted Date
2024-03-15
Lead Sponsor
Cardiology Research UBC
Target Recruit Count
18
Registration Number
NCT02008786
Locations
🇨🇦

Vancouver General Hospital, Vancouver, British Columbia, Canada

Evaluating of Pharmacokinetic Profile of BCWP_C003 and Co-administration of Rosuvastatin and Metformin

Phase 1
Completed
Conditions
Interventions
First Posted Date
2013-11-25
Last Posted Date
2017-07-17
Lead Sponsor
BC World Pharm Co. Ltd.
Target Recruit Count
35
Registration Number
NCT01992211
Locations
🇰🇷

Seoul National University Hospital, Seoul, Korea, Republic of

A Study to Evaluate the Efficacy and Safety of Rosuvastatin in Hypercholesterolemia.

Not Applicable
Conditions
Interventions
First Posted Date
2013-11-13
Last Posted Date
2013-11-13
Lead Sponsor
Pin Siang Medical Biotechnology Co., Ltd.
Target Recruit Count
40
Registration Number
NCT01982461
Locations
🇨🇳

Tri-Service General Hospital, Taipei, Taiwan

Rosuvastatin in African Americans With Cerebrovascular Disease

Phase 4
Terminated
Conditions
Interventions
First Posted Date
2013-11-03
Last Posted Date
2013-11-05
Lead Sponsor
Wayne State University
Target Recruit Count
20
Registration Number
NCT01975194
Locations
🇺🇸

Detroit Medical Center, Detroit, Michigan, United States

Impact of High-dose Pretreatment of Rosuvastatin in Patients With Acute Coronary Syndrome Following Off-pump Coronary Artery Bypass: Results From the HIROP-ACS (HIgh-dose Pretreatment of Rosuvastatin During Off-Pump Coronary Bypass in Acute Coronary Syndrome) Study

First Posted Date
2013-10-29
Last Posted Date
2013-11-01
Lead Sponsor
Yonsei University
Target Recruit Count
234
Registration Number
NCT01971606
Locations
🇰🇷

Division of Cardiovascular Surgery, Severance Cardiovascular Hospital , Yonsei University College of Medicine, Seoul, Korea, Republic of

TA-8995: Its Use in Patients With Mild Dyslipidaemia (TULIP)

First Posted Date
2013-10-28
Last Posted Date
2014-08-21
Lead Sponsor
Xention Ltd
Target Recruit Count
364
Registration Number
NCT01970215
Locations
🇳🇱

Albert Schweitzer Ziekenhuis, Sliedrecht, Netherlands

🇳🇱

Andromed Zoetermeer, Leiderdorp, Netherlands

🇳🇱

Andromed Breda B.V, Breda, Netherlands

and more 14 locations

Randomized Trial of Creatine-kinase Leak After Rosuvastatin At the Time of Percutaneous Coronary Intervention

Phase 4
Conditions
Interventions
First Posted Date
2013-10-24
Last Posted Date
2013-10-24
Lead Sponsor
Kleber Bomfim Araujo Martins
Target Recruit Count
528
Registration Number
NCT01968577
Locations
🇧🇷

Instituto Dante Pazzanese de Cardiologia, Sao Paulo, Brazil

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