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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

PREPARE (A5361s) Ancillary Study of REPRIEVE (A5332)

Phase 3
Completed
Conditions
HIV-1 Infection
Interventions
Drug: Placebos
First Posted Date
2017-03-03
Last Posted Date
2024-10-28
Lead Sponsor
Advancing Clinical Therapeutics Globally for HIV/AIDS and Other Infections
Target Recruit Count
602
Registration Number
NCT03070223
Locations
🇺🇸

Alabama CRS (31788), Birmingham, Alabama, United States

🇺🇸

University of Southern California (1201), Los Angeles, California, United States

🇺🇸

University of California, Los Angeles CARE Center CRS (601), Los Angeles, California, United States

and more 28 locations

Dyslipidemia of Obesity Intervention in Teens

Phase 3
Completed
Conditions
Dyslipidemia
Obesity
Interventions
Drug: Placebo
First Posted Date
2016-11-06
Last Posted Date
2024-07-05
Lead Sponsor
Carelon Research
Target Recruit Count
122
Registration Number
NCT02956590
Locations
🇺🇸

The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, United States

🇺🇸

University of Wisconsin, Madison, Wisconsin, United States

🇨🇦

The Hospital for Sick Children, Toronto, Ontario, Canada

and more 13 locations

Effect of High-dose Pitavastatin on Glucose Control in Patients With Metabolic Syndrome

First Posted Date
2016-10-20
Last Posted Date
2017-02-09
Lead Sponsor
Seoul National University Hospital
Target Recruit Count
500
Registration Number
NCT02940366
Locations
🇰🇷

Seoul National University Hospital, Seoul, Korea, Republic of

A Drug-Drug Interaction Study to Evaluate the Effect of AL-794 on the Pharmacokinetics of Oseltamivir and JNJ-63623872

First Posted Date
2016-09-05
Last Posted Date
2025-02-03
Lead Sponsor
Alios Biopharma Inc.
Target Recruit Count
68
Registration Number
NCT02888327
Locations
🇬🇧

Hammersmith Medicines Research, London, United Kingdom

Effect of Pitavastatin on Erythrocyte Membrane Fatty Acid Contents in Patients With Chronic Kidney Disease

Phase 4
Completed
Conditions
Chronic Kidney Disease
Interventions
First Posted Date
2016-08-11
Last Posted Date
2021-09-21
Lead Sponsor
Dong-A University
Target Recruit Count
45
Registration Number
NCT02863185
Locations
🇰🇷

Won Suk An, Busan, Korea, Republic of

🇰🇷

Dong-A University, Busan, Korea, Republic of

Efficacy & Long-term Safety Comparison Study of NK-104-CR & Livalo® IR With Primary Hyperlipidemia or Mixed Dyslipidemia

Phase 3
Withdrawn
Conditions
Hyperlipidemia
Dyslipidemia
Interventions
Drug: NK-104-CR
Drug: Placebo (for NK-104-CR)
Drug: Placebo (for Livalo® IR)
First Posted Date
2016-06-15
Last Posted Date
2021-05-10
Lead Sponsor
Kowa Research Institute, Inc.
Registration Number
NCT02799758

Drug Transporter Interaction Study PHENTRA_2015_KPUK

First Posted Date
2016-04-19
Last Posted Date
2019-09-10
Lead Sponsor
University of Cologne
Target Recruit Count
24
Registration Number
NCT02743260
Locations
🇩🇪

Department of Pharmacology I, University Hospital Cologne, Cologne, NRW, Germany

Safety and Efficacy Comparison Study of NK-104-CR (Controled Release) in Patients With Primary Hyperlipidemia or Mixed Dyslipidemia

Phase 3
Withdrawn
Conditions
Hyperlipidemia
Dyslipidemia
Interventions
Drug: NK-104-CR
Drug: Placebo
First Posted Date
2016-02-01
Last Posted Date
2021-05-10
Lead Sponsor
Kowa Research Institute, Inc.
Registration Number
NCT02670434

A Study to Investigate the Effect of JNJ-63623872 on Pitavastatin in Healthy Participants

Phase 1
Completed
Conditions
Healthy
Interventions
First Posted Date
2015-11-03
Last Posted Date
2016-01-27
Lead Sponsor
Janssen Research & Development, LLC
Target Recruit Count
14
Registration Number
NCT02595268

Effect of Low-dose vs. High-dose Pitavastatin on In-stent Restenosis

Phase 4
Completed
Conditions
Angina
Atherosclerosis
Neointima
Interventions
First Posted Date
2015-09-09
Last Posted Date
2020-11-10
Lead Sponsor
Korea University Anam Hospital
Target Recruit Count
1000
Registration Number
NCT02545231
Locations
🇰🇷

Korea University Anam Hospital, Seoul, Korea, Republic of

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