Fluvastatin sodium

"目录号: HY-14664A

Metabolic Enzyme/ProteaseAutophagy-

Fluvastatin钠是HMG-CoA还原酶竞争性抑制剂。

HMG-CoA Reductase (HMGCR)Autophagy

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生物活性

Description

Fluvastatin sodium is a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), used to treat hypercholesterolemia and to prevent cardiovascular disease.Target: HMGCR Fluvastatin is a competitive inhibitor of hydroxymethylglutaryl-coenzyme A reductase (HMGCR), the enzyme that catalyzes the conversion of HMG-CoA to mevalonic acid, the rate-limiting step in cholesterol biosynthesis. Human hepatocellular carcinoma cell (HCC) studies indicate that Fluvastatin induces G2/M phase arrest. In the presence of Fluvastatin, HCC cells show a decrease of Bcl-2 and procaspase-9 expression, and an increase in Bax, cleaved caspase-3, and cytochrome c. Fluvastatin is antilipemic and is used to reduce plasma cholesterol levels and prevent cardiovascular disease.

Clinical Trial

NCT00664742

Novartis

Metabolic Syndrome

September 2006

Phase 4

NCT01551173

Novartis Pharmaceuticals-Novartis

Lipid Metabolism Disorders

January 2012

Phase 4

NCT00674297

Hospital for Special Surgery, New York-University of Texas

Antiphospholipid Syndrome

May 2008

Phase 2

NCT03189511

Irene Burger-University of Basel-University of Zurich

Adipose Tissue, Brown-Insulin Resistance-Clinical Trial

May 31, 2017

Phase 4

NCT00752843

Corcept Therapeutics

Healthy Subjects

September 2008

Phase 1

NCT00814723

Medical University of Graz

Hypercholesterolemia

September 2005

Phase 4

NCT00565474

Novartis Pharmaceuticals-Novartis

Graft Vasculopathy

September 2001

Phase 4

NCT00421005

University of Bologna

Heart Transplantation-Hypercholesterolemia

November 2004

Phase 4

NCT00487318

Bader, Ted, M.D.-VA Office of Research and Development

Chronic Hepatitis C

June 2007

Phase 2

NCT01681199

Beijing Anzhen Hospital-Novartis

Coronary Heart Disease-Atherosclerosis

July 2012

Phase 4

NCT00814606

University of Chicago

Hepatitis C-Hepatitis C Virus

February 2010

Phase 2

NCT00138528

Novartis

Metabolic Syndrome

October 2004

Phase 4

NCT00441493

Bader, Ted, M.D.-VA Office of Research and Development

Hepatitis C

September 2006

NCT00171262

Novartis

Dyslipidemia

August 2004

Phase 4

NCT00404287

AORTICA Group

Aortic Valve Stenosis

October 2006

Phase 4

NCT00223041

University of Schleswig-Holstein

Renal Transplantation

April 2003

Phase 2-Phase 3

NCT00136799

Novartis

Mixed Dyslipidemia-Hypercholesterolemia

June 2005

Phase 3

NCT00171275

Novartis-Ministry of Health, Czech Republic

Coronary Disease-Myocardial Infarction

November 2003

Phase 4

NCT00125125

Novartis

Dyslipidemia

May 2005

Phase 4

NCT00171327

Novartis

Hypertension-Dyslipidemia

July 2004

Phase 4

NCT00171236

Novartis

Heterozygous Familial Hypercholesterolemia-Mixed Dyslipidemia

October 2001

Phase 3

NCT00416403

University of California, San Francisco-National Cancer Institute (NCI)

Breast Cancer

July 2006

Phase 2

NCT00465322

University Hospital Inselspital, Berne

Drug-Interactions

Phase 4

NCT00489424

Novartis Pharmaceuticals-Novartis

Osteoporosis

June 2007

Phase 4

NCT00382161

University Hospital, Saarland-Novartis

Impotence

October 2006

Phase 3

NCT00171288

Novartis

Dyslipidemia

August 2003

Phase 3

NCT00223028

University of Schleswig-Holstein

Renal Transplantation

April 2005

Phase 4

NCT00385658

Novartis

Dyslipidemia

August 2006

Phase 4

NCT00549926

Yokohama City University Medical Center

Coronary Disease-Hypercholesterolemia

October 2007

Phase 4

NCT01992042

University Health Network, Toronto

Prostate Cancer

February 2014

Phase 2

NCT00223015

University of Schleswig-Holstein

Renal Transplantation

May 2004

Phase 4

NCT02115074

Centre Oscar Lambret-Reliable Cancer Therapies

Glioma

June 2014

Phase 1

NCT00821574

Novartis

Hypertension, Dyslypidaemia

July 2005

Phase 4

NCT00199927

Mario Negri Institute for Pharmacological Research

Chronic Nephropathy-Proteinuria-Hypertension

March 2003

Phase 3

NCT00176410

University of Leipzig-Novartis

Aortic Valve Stenosis

January 2003

Phase 2

NCT01045512

Martin-Luther-Universität Halle-Wittenberg-Novartis

Aging-Inflammation

October 2009

Phase 2

NCT00407680

Kitasato University-Tokai University-Yokohama City University Medical Center-St. Marianna University School of Medicine

Type 2 Diabetes Mellitus-Hypertension

October 2006

Phase 4

NCT00309257

Mario Negri Institute for Pharmacological Research

Alport Syndrome

January 2004

Phase 2

NCT00718796

The Canadian College of Naturopathic Medicine-Canada Post Corporation-Canadian Union of Postal Workers

Cardiovascular Disease

April 2008

Phase 3

NCT02518516

Canadian Network for Observational Drug Effect Studies, CNODES-Drug Safety and Effectiveness Network, Canada-Canadian Institutes of Health Research (CIHR)

Hypercholesterolemia

January 2011

NCT02518503

Canadian Network for Observational Drug Effect Studies, CNODES-Drug Safety and Effectiveness Network, Canada-Canadian Institutes of Health Research (CIHR)

Diabetes Mellitus, Type 2-Cardiovascular Disease

July 2012

NCT00132717

Merck Sharp & Dohme Corp.

Hypercholesterolemia

January 1, 2005

Phase 3

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References

[1].Araújo FA, Rocha MA, Capettini LS, et al. 3-Hydroxy-3-methylglutaryl coenzyme A reductase inhibitor (fluvastatin) decreases inflammatory angiogenesis in mice. APMIS. 2012 24. [Epub ahead of print]

[2].Makabe S, Takahashi Y, Watanabe H, et al. Fluvastatin protects vascular smooth muscle cells against oxidative stress through the Nrf2-dependent antioxidant pathway. Atherosclerosis. 2010 Dec;213(2):377-84.

[3].Zhang W, Wu J, Zhou L, et al. Fluvastatin, a lipophilic statin, induces apoptosis in human hepatocellular carcinoma cells through mitochondria-operated pathway. Indian J Exp Biol. 2010 Dec;48(12):1167-74.

[4].Scripture CD, Pieper JA. Clinical pharmacokinetics of fluvastatin. Clin Pharmacokinet. 2001;40(4):263-81.

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