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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 Lipid Profiles in HIV-infected Patients With Dyslipidemia and Receiving Atazanavir/Ritonavir

Phase 4
Completed
Conditions
HIV
Dyslipidemia
Interventions
Drug: placebo
First Posted Date
2015-05-13
Last Posted Date
2016-10-10
Lead Sponsor
Ramathibodi Hospital
Target Recruit Count
24
Registration Number
NCT02442700

Evaluating the Use of Pitavastatin to Reduce the Risk of Cardiovascular Disease in HIV-Infected Adults

Phase 3
Completed
Conditions
HIV
Cardiovascular Diseases
Interventions
Drug: Placebo
First Posted Date
2015-01-22
Last Posted Date
2024-10-18
Lead Sponsor
National Institute of Allergy and Infectious Diseases (NIAID)
Target Recruit Count
7769
Registration Number
NCT02344290
Locations
🇺🇸

Alabama CRS*, Birmingham, Alabama, United States

🇺🇸

University of Southern California CRS*, Los Angeles, California, United States

🇺🇸

UCLA CARE Center CRS*, Los Angeles, California, United States

and more 134 locations

Effects of Pitavastatin on Insulin Sensitivity and Liver Fat

Not Applicable
Completed
Conditions
Obesity
Fatty Liver, Nonalcoholic
Interventions
Other: PLACEBO
First Posted Date
2014-11-13
Last Posted Date
2019-07-02
Lead Sponsor
Massachusetts General Hospital
Target Recruit Count
50
Registration Number
NCT02290106
Locations
🇺🇸

Massachusetts General Hospital, Boston, Massachusetts, United States

Effect of Pitavastatin on Coronary Flow Reserve in Hypertensive Patients

Phase 4
Completed
Conditions
Hypertension
Cardiovascular Risk
Interventions
Other: Control
First Posted Date
2014-05-22
Last Posted Date
2016-10-14
Lead Sponsor
Asan Medical Center
Target Recruit Count
85
Registration Number
NCT02144922
Locations
🇰🇷

Asan Medical Center, Seoul, Korea, Republic of

to Evaluate the Safety and Efficacy of Pitavastatin in Patients With IFG and Hyperlipidemia

Phase 4
Completed
Conditions
HbA1c Level Associated With Lipid Compositions
Interventions
First Posted Date
2014-02-06
Last Posted Date
2018-03-08
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
313
Registration Number
NCT02056847
Locations
🇰🇷

JW pharmaceutical, Seoul, Korea, Republic of

Preventive Effect of Pitavastatin on Contrast-Induced Nephropathy in Patients With Renal Dysfunction

Phase 4
Conditions
Contrast-induced Nephropathy
Interventions
Drug: Placebo
First Posted Date
2013-06-07
Last Posted Date
2013-06-07
Lead Sponsor
Gachon University Gil Medical Center
Target Recruit Count
404
Registration Number
NCT01871792
Locations
🇰🇷

Gachon University Gil Hospital, Incheon, Korea, Republic of

Evaluation of Pharmacokinetic Interaction Between Micronized Fenofibrate and Pitavastatin

First Posted Date
2013-01-14
Last Posted Date
2018-08-03
Lead Sponsor
Hanlim Pharm. Co., Ltd.
Target Recruit Count
24
Registration Number
NCT01767610
Locations
🇰🇷

Kyungpook National University Hospital, Daegu, Korea, Republic of

Pharmacokinetic Study of Livalo® Fixed Combination Drug in Healthy Subjects

Phase 1
Completed
Conditions
Hyperlipidemia
Hypertension
Interventions
Drug: Pitavastatin, Valsartan
First Posted Date
2013-01-09
Last Posted Date
2017-03-10
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
52
Registration Number
NCT01764178
Locations
🇰🇷

Asan Medical Center, Seoul, Korea, Republic of

Pharmacokinetic Study of Pitavastatin and Ritonavir-Boosted Darunavir or Efavirenz

Phase 1
Completed
Conditions
HIV
Hyperlipidemia
Interventions
First Posted Date
2012-09-28
Last Posted Date
2020-08-11
Lead Sponsor
NYU Langone Health
Target Recruit Count
34
Registration Number
NCT01695954
Locations
🇺🇸

Bellevue/NYU AIDS Clinical Trials Unit, New York, New York, United States

PharmacOdynamic compaRison of piTavastatin Versus atOrvastatin on Platelet Reactivity

Phase 4
Conditions
Coronary Artery Disease
Interventions
First Posted Date
2012-07-24
Last Posted Date
2013-03-07
Lead Sponsor
University of Roma La Sapienza
Target Recruit Count
100
Registration Number
NCT01648829
Locations
🇮🇹

Sapienza University, Rome, Italy

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