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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

Safety, Tolerability, and Pharmacokinetic of Single Dose of Pitavastatin 4 mg in Severe Renal Patients Versus Healthy Adult Volunteers

Phase 4
Completed
Conditions
Severe Renal Impairment
Interventions
First Posted Date
2010-01-06
Last Posted Date
2012-08-13
Lead Sponsor
Kowa Research Institute, Inc.
Target Recruit Count
16
Registration Number
NCT01043094

Randomized Evaluation of Aggressive or Moderate Lipid Lowering Therapy With Pitavastatin in Coronary Artery Disease (REAL-CAD)

Not Applicable
Completed
Conditions
Coronary Artery Disease
Interventions
First Posted Date
2010-01-06
Last Posted Date
2021-05-17
Lead Sponsor
Juntendo University
Target Recruit Count
13054
Registration Number
NCT01042730
Locations
🇯🇵

Kyoto University Hospital, Kyoto, Japan

🇯🇵

Juntendo University School of Medicine, Tokyo, Japan

Efficacy and Safety Study of Pitavastatin Compared to atoRvastatin in Type 2 dIabeTes Mellitus With Hypercholesterolemia

Phase 4
Completed
Conditions
Hypercholesterolemia With Type2DM
Interventions
First Posted Date
2009-04-28
Last Posted Date
2019-09-17
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
161
Registration Number
NCT00889226

Comparison of Pitavastatin With Atorvastatin in Increasing High Density Lipoprotein - Cholesterol (HDL-C) and Adiponectin in Patients With Dyslipidemia and Coronary Artery Disease (CAD)

Phase 4
Completed
Conditions
Hypercholesterolemia
Coronary Artery Disease
Interventions
First Posted Date
2009-03-16
Last Posted Date
2013-10-14
Lead Sponsor
Kumamoto University
Target Recruit Count
129
Registration Number
NCT00861861
Locations
🇯🇵

Kumamoto University Graduate School of Medical Sciences Department of Cardiocascular Medicine, Kumamoto, Japan

Differential Intervention Trial by Standard Therapy Versus Pitavastatin in Patients With Chronic Hemodialysis (DIALYSIS)

Not Applicable
Terminated
Conditions
Cardiovascular Disease
Interventions
First Posted Date
2009-02-18
Last Posted Date
2021-08-30
Lead Sponsor
Chieko Hamada
Target Recruit Count
905
Registration Number
NCT00846118
Locations
🇯🇵

Division of Nephrology, Department of Internal Medicine, Juntendo Hospital, Tokyo, Japan

Pitavastatin Pre-Treatment Study in Patient With Elective PCI for Stable Angina Pectoris (PIPA)

Phase 4
Withdrawn
Conditions
Percutaneous Coronary Intervention
Interventions
First Posted Date
2008-11-06
Last Posted Date
2012-03-30
Lead Sponsor
JW Pharmaceutical
Registration Number
NCT00786734
Locations
🇰🇷

Catholic University of Korea Kangnam St. Mary's Hospital, Seoul, Korea, Republic of

Effects of Statins on the Pharmacokinetics for Midazolam in Healthy Volunteers

Not Applicable
Completed
Conditions
Healthy Volunteers
Interventions
First Posted Date
2008-07-16
Last Posted Date
2011-09-07
Lead Sponsor
Hamamatsu University
Target Recruit Count
11
Registration Number
NCT00716846
Locations
🇯🇵

Hamamatsu University School of Medicine, Hamamatsu, Japan

Pitavastatin on Carotid Intima-media Thickness

Not Applicable
Conditions
Hyperlipidemia
Carotid Artery Diseases
Interventions
First Posted Date
2008-07-09
Last Posted Date
2009-09-10
Lead Sponsor
Kyoto Prefectural University of Medicine
Target Recruit Count
300
Registration Number
NCT00711919
Locations
🇯🇵

Ayabe City Hospital, Ayabe, Kyoto, Japan

🇯🇵

Tanabe Central Hospital, Kyotanabe, Kyoto, Japan

🇯🇵

Maizuru Kyosai Hospital, Maizuru, Kyoto, Japan

and more 15 locations

South Korean Pitavastatin Heart Failure Study

Phase 4
Completed
Conditions
Chronic Heart Failure
Interventions
First Posted Date
2008-06-19
Last Posted Date
2014-05-14
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
70
Registration Number
NCT00701285
Locations
🇰🇷

SEOUL St. Mary's Hospital, Seoul, Seocho-Ku, Korea, Republic of

Evaluation of Potential for Drug Interaction Between SCH 58235 (Ezetimibe) and Pitavastatin (Study P03962)(COMPLETED)

Phase 1
Completed
Conditions
Hypercholesterolemia
Interventions
First Posted Date
2008-04-07
Last Posted Date
2022-02-16
Lead Sponsor
Organon and Co
Target Recruit Count
18
Registration Number
NCT00653913
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