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Pitavastatin

Generic Name
Pitavastatin
Brand Names
Livalo, Zypitamag
Drug Type
Small Molecule
Chemical Formula
C25H24FNO4
CAS Number
147511-69-1
Unique Ingredient Identifier
M5681Q5F9P
Background

Pitavastatin, also known as the brand name product Livalo, is a lipid-lowering drug belonging to the statin class of medications. By inhibiting the endogenous production of cholesterol within the liver, statins lower abnormal cholesterol and lipid levels and ultimately reduce the risk of cardiovascular disease. More specifically, statin medications competitively inhibit the enzyme hydroxymethylglutaryl-coenzyme A (HMG-CoA) Reductase, which catalyzes the conversion of HMG-CoA to mevalonic acid. This 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.

Pitavastatin and other drugs from the statin class of medications including atorvastatin, pravastatin, rosuvastatin, fluvastatin, and lovastatin are considered first-line options for the treatment of dyslipidemia. Increasing use of the statin class of drugs 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% decrease in LDL cholesterol levels. Study data has confirmed that pitavastatin's potency in lowering LDL-C is comparable to that of other statins but also has increased efficacy in increasing HDL-C (also known as "good cholesterol"). Despite these differences in potency, several trials have demonstrated only minimal differences in terms of clinical outcomes between statins.

Indication

用于治疗高胆固醇症(高脂血症)、家族性高胆固醇症。

Associated Conditions
Apolipoprotein B increased, Elevation of serum triglyceride levels, Increases in serum total low-density lipoprotein (LDL), Increases in total cholesterol

Effects of Pitavastatin on Monocyte, Endothelial Dysfunction and HDL-C in Subjects With Metabolic Syndrome

Phase 1
Completed
Conditions
Metabolic Syndrome
Interventions
First Posted Date
2012-05-10
Last Posted Date
2013-07-22
Lead Sponsor
Kowa Research Europe
Target Recruit Count
14
Registration Number
NCT01595828
Locations
🇬🇧

Kowa Research Europe Ltd., Wokingham, United Kingdom

Neointimal Coverage After Implantation of Biolimus Eluting Stent With Biodegradable Polymer: Optical Coherence Tomographic Assessment According to the Treatment of Dyslipidemia and Hypertension and the Types of Implanted Drug-eluting Stents

Phase 4
Completed
Conditions
Stable Angina or Acute Coronary Syndrome Considered for Percutaneous Coronary Intervention With Dyslipidemia or Hypertension
Interventions
Device: Sirolimus-eluting stent
Device: Biolimus-eluting stents
Drug: Non-ARB /day after DES implantation
Drug: Eposartan 600mg/day after DES implantation
First Posted Date
2012-01-02
Last Posted Date
2016-07-27
Lead Sponsor
Yonsei University
Target Recruit Count
120
Registration Number
NCT01502904
Locations
🇰🇷

Severance Hospital, Seoul, Korea, Republic of

Drug-Drug Interaction of Cardizem LA (Diltiazem Hydrochloride) on Pitavastatin

Phase 4
Completed
Conditions
Healthy
Interventions
First Posted Date
2011-08-24
Last Posted Date
2012-07-13
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
28
Registration Number
NCT01422382

Drug-Drug Interaction of Darunavir/Ritonavir on Pitavastatin

Phase 4
Completed
Conditions
Healthy
Interventions
Drug: Darunavir/Ritonavir (Prezista)
First Posted Date
2011-08-24
Last Posted Date
2012-07-13
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
28
Registration Number
NCT01422369

Pharmacokinetic Study of Livalo® Fixed Combination Drug in Healthy Subjects

Phase 1
Completed
Conditions
Hyperlipidemia
Hypertension
Interventions
Drug: Pitavastatin, Valsartan
First Posted Date
2011-08-01
Last Posted Date
2013-01-03
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
48
Registration Number
NCT01406431
Locations
🇰🇷

Asan Medical Center, Seoul, Korea, Republic of

Efficacy and Safety Study of Pitavastatin and Atorvastatin in High Risk Hypercholesterolemic Patients

Phase 3
Conditions
Hyperlipidemia
Interventions
First Posted Date
2011-07-01
Last Posted Date
2011-07-01
Lead Sponsor
Tai Tien Pharmaceuticals Co., Ltd.
Target Recruit Count
200
Registration Number
NCT01386853
Locations
🇨🇳

Taipei Veterans General Hospital, Taipei, Taiwan

🇨🇳

Tri-Service General Hospital, Taipei, Taiwan

🇨🇳

National Cheng Kung University Hospital, Tainan, Taiwan

and more 3 locations

A 12-Week Study Comparing Pitavastatin 4 mg vs. Pravastatin 40 mg in HIV-Infected Subjects

Phase 4
Completed
Conditions
Dyslipidemia
Interventions
First Posted Date
2011-02-23
Last Posted Date
2014-04-29
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
252
Registration Number
NCT01301066

Prevail-Us: A Study Of Pitavastatin 4 mg Vs. Pravastatin 40 mg In Patients With Primary Hyperlipidemia Or Mixed Dyslipidemia

Phase 4
Completed
Conditions
Primary Dyslipidemia
Mixed Dyslipidemia
Interventions
First Posted Date
2010-12-08
Last Posted Date
2012-05-08
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
328
Registration Number
NCT01256476

Efficacy and Safety Study of Pitavastatin Versus Atorvastatin to Treat Hypercholesterolemia

Phase 4
Completed
Conditions
Hypercholesterolemia
Interventions
First Posted Date
2010-07-21
Last Posted Date
2022-04-11
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
200
Registration Number
NCT01166633

Drug-Drug Interaction of Lopinavir/Ritonavir on Pitavastatin

Phase 4
Completed
Conditions
Healthy Volunteers
Interventions
First Posted Date
2010-01-27
Last Posted Date
2021-06-22
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
24
Registration Number
NCT01057433
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