MedPath

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

Efficacy of Statin Addition to Neoadjuvant Chemotherapy Protocols for Breast Cancer

Phase 2
Conditions
Breast Cancer
Interventions
Drug: placebo
First Posted Date
2021-01-12
Last Posted Date
2021-01-12
Lead Sponsor
Mansoura University
Target Recruit Count
60
Registration Number
NCT04705909
Locations
🇪🇬

Faculty of pharmacy, Mansoura university, Mansoura, Egypt

Compare the Efficacy and Safety of 1PC111 With Pitavastatin and Ezetimibe in Patients With Primary Hypercholesterolemia or Mixed Dyslipidemia

Phase 3
Completed
Conditions
Primary Hypercholesterolemia
Mixed Dyslipidemias
Interventions
First Posted Date
2020-11-24
Last Posted Date
2022-05-18
Lead Sponsor
Orient Pharma Co., Ltd.
Target Recruit Count
390
Registration Number
NCT04643093
Locations
🇨🇳

E-Da Hospital, Kaohsiung, Taiwan

🇨🇳

National Taiwan University Hospital, Taipei, Taiwan

🇨🇳

Tri-Service General Hospital, Taipei, Taiwan

and more 31 locations

Pitavastatin in Combination With Venetoclax for Chronic Lymphocytic Leukemia or Acute Myeloid Leukemia

Phase 1
Active, not recruiting
Conditions
Acute Myeloid Leukemia
Chronic Lymphocytic Leukemia
AML, Adult
CLL
CLL, Relapsed
CLL, Refractory
Interventions
First Posted Date
2020-08-13
Last Posted Date
2024-10-21
Lead Sponsor
University of California, Irvine
Target Recruit Count
6
Registration Number
NCT04512105
Locations
🇺🇸

Chao Family Comprehensive Cancer Center, University of California, Irvine, Orange, California, United States

Efficacy and Safety of Pitavastatin in a Real-world Setting

Completed
Conditions
Hypercholesterolemia
First Posted Date
2020-05-26
Last Posted Date
2021-04-19
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
28343
Registration Number
NCT04402112

The Occurrence of MACE in Patients With AMI Receiving Pitavastatin/Valsartan Treatment

Conditions
Hypercholesterolemia
First Posted Date
2020-02-17
Last Posted Date
2021-04-13
Lead Sponsor
JW Pharmaceutical
Target Recruit Count
905
Registration Number
NCT04270344
Locations
🇰🇷

JWP, Seoul, Seocho-gu, Korea, Republic of

A Study to Investigate the Effect of RO7049389 on the Pharmacokinetics of Pitavastatin in Healthy Volunteers

Phase 1
Completed
Conditions
Healthy Volunteers
Interventions
First Posted Date
2018-10-24
Last Posted Date
2020-01-10
Lead Sponsor
Hoffmann-La Roche
Target Recruit Count
18
Registration Number
NCT03717064
Locations
🇺🇸

Covance Research Unit - Daytona, Daytona Beach, Florida, United States

A Clinical Trial to Evaluate the Efficacy and Safety of Pitavastatin/Fenofibrate in Complex-dyslipidemia

Phase 3
Completed
Conditions
Complex-dyslipidemia
Interventions
Drug: HL-PIF cap.160/2mg + Placebo
First Posted Date
2018-08-07
Last Posted Date
2018-08-07
Lead Sponsor
Hanlim Pharm. Co., Ltd.
Target Recruit Count
347
Registration Number
NCT03618797

Thyroid Hormone Replacement for Subclinical Hypothyroidism and Dyslipidemia in ASCVD (ThyroHeart-Lipid Study)

Not Applicable
Conditions
Subclinical hypothyroïdism
Statin
Dyslipidemia
ASCVD
Interventions
First Posted Date
2018-07-31
Last Posted Date
2019-03-20
Lead Sponsor
Shaochun.Li
Target Recruit Count
248
Registration Number
NCT03606824
Locations
🇨🇳

Fuwai Hospital, China National Center for Cardiovascular Diseases, Beijing, China

China Protection Trial of Glucose Metabolism by Pitavastatin in Patients With Prediabetes and Hypertension

Phase 4
Conditions
Prediabetic State
Hypertension
Dyslipidemias
Interventions
First Posted Date
2018-05-22
Last Posted Date
2019-06-03
Lead Sponsor
Jun Tao
Target Recruit Count
396
Registration Number
NCT03532620
Locations
🇨🇳

First Affiliated Hospital of Zhengzhou University, Zhengzhou, Henan, China

🇨🇳

Fourth People's Hospital of Chongqing, Chongqing, Chongqing, China

🇨🇳

First Affiliated Hospital,Sun Yat-sen University, Guangzhou, Guangdong, China

and more 10 locations

Safety and Efficacy of Statins for Chinese Patients With Dyslipidemia

Phase 4
Conditions
Dyslipidemias
Interventions
First Posted Date
2018-02-01
Last Posted Date
2018-02-01
Lead Sponsor
Fudan University
Target Recruit Count
10000
Registration Number
NCT03418974
Locations
🇨🇳

School of Public Health, Fudan University, Shanghai, Shanghai, China

🇨🇳

Heart Center of Peking University People's Hospital, Beijing, Beijing, China

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