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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00249249
Other study ID # NK-104-301
Secondary ID EudraCT number 2
Status Completed
Phase Phase 3
First received November 4, 2005
Last updated January 7, 2010
Start date October 2005
Est. completion date November 2006

Study information

Verified date January 2010
Source Kowa Research Europe
Contact n/a
Is FDA regulated No
Health authority Spain: Spanish Agency of MedicinesIndia: Indian Council of Medical ResearchRussia: Pharmacological Committee, Ministry of Health
Study type Interventional

Clinical Trial Summary

The purpose of this study is to compare the efficacy of pitavastatin with that of atorvastatin.


Description:

Following a wash-out dietary lead-in period, patients will receive either Atorvastatin or Pitavastatin during 12 weeks, in order to establish the efficacy of pitavastatin in reducing cholesterol levels.


Recruitment information / eligibility

Status Completed
Enrollment 830
Est. completion date November 2006
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 75 Years
Eligibility Inclusion Criteria:

- Males and females (age 18-75 years).

- Non-pregnant, non-lactating females

- Women of child bearing potential should use sustained contraceptive preparations or an approved mechanical contraceptive method.

- Eligible and able to participate and have given informed consent

- Must have been following a restrictive diet and does not eat or drink grapefruit

- Diagnosis of primary hypercholesterolemia or combined dyslipidemia

- Available for every clinic visit, which will occur in the morning.

Exclusion Criteria:

- Homozygous familial hypercholesterolemia or familial hypoalphalipoproteinemia

- Conditions which may cause secondary dyslipidemia.

- Condition which might significantly alter the absorption, distribution, metabolism, or excretion of any drug.

- History of pancreatic injury or pancreatitis, or impaired pancreatic function/injury

- Liver injury

- Impaired renal function

- Current obstruction of the urinary tract or difficulty in voiding due to mechanical as well as inflammatory conditions, which is likely to require intervention during the course of the study or is regarded as clinically meaningful by the investigator

- Serum creatine kinase (CK) >5 x upper limit of the reference range (ULRR).

- Uncontrolled hypothyroidism

- Severe acute illness or severe trauma in the last 3 months

- Major surgery, 3 months prior to Visit 1

- Significant cardiovascular disease (CVD) prior to randomization

- Evidence of symptomatic heart failure, gross cardiac enlargement; significant heart block or cardiac arrhythmias. History of uncontrolled complex ventricular arrhythmias, uncontrolled atrial fibrillation/flutter or uncontrolled supraventricular tachycardias with a ventricular response rate of >100 beats per minute at rest.

- Left ventricular (LV) ejection fraction < 0.25

- History of symptomatic cerebrovascular disease

- Conditions at the discretion of the investigator

- Known HIV infection

- Poorly controlled or uncontrolled hypertension.

- Known muscular or neuromuscular disease of any type

- Neoplastic disease

- Drug abuse or continuous consumption of more than 65 mL pure alcohol per day

- Exposure to any investigational new drug within 30 days of study entry or ingestion of any drug known to be toxic to a major organ system

- Current or recent use of supplements known to alter lipid metabolism

- Hypersensitivity reactions to other HMG-CoA reductase inhibitors

- Concomitant medication not permitted

- Resistant to lipid-lowering medications. Known hypersensitivity or intolerance to any lipid lowering agent

- Excessive obesity

- Regular clinic attendance in the morning impractical

- Signs of mental dysfunction or other factors likely to limit ability to cooperate

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double-Blind, Primary Purpose: Treatment


Intervention

Drug:
Pitavastatin

Atorvastatin


Locations

Country Name City State
Denmark Copenhagen University Hospital Copenhagen
Denmark Medical Center Copenhagen
Denmark Y Forskning, Bispebjerg Hospital Copenhagen Nv
Denmark Frederiks Hospital, Kardiologisk Frederiksberg
Denmark Kolesterollaboratoriet Hellerup
Denmark CCBR A/S Vejle
Finland Geri-Med Oy Helsinki
Finland Kaisaniemen Laakariasema Helsinki
Finland keravan Laakarikeskus Helsinki
Finland SOK-tyoterveyshuolto Tampere
Finland TYKS University Hospital Turku
Germany Kardiologische Gemeinschaftspraxis Prof. Reifart Bad Soden/Taunus
Germany Praxis Dr. Boenninghoff Beckum
Germany Klinische Forschung Berlin Mitte Berlin
Germany Gemeinschaftspraxis am Bahnhof Berlin-Spandau
Germany Pharmakologisches Studienzentum Chemnitz Chemnitz
Germany GWT-TUK mbH, Zentrum fur Klinische Studien Dresden
Germany Internistische Diabetische Schwerpunktpraxis Dr. Frankfurt Am Main
Germany Gemeinschaftspraxis Dr. Krause, Th. Menke Goch
Germany Klinische Forschung Hamburg Hamburg
Germany Innere Medizin I/Medizinische Klinik Heidelberg
Germany Gemeinschaftspraxis H. Holz Dr. Med, K. W. Klingl Lampertheim
Germany ZET-Studien GmbH Leipzig Leipzig
Germany Internistische Gemeinschaftspraxis Mainz
Germany Praxis Dr. Wachter Mannheim
Germany Gemeinschaftspraxis Melcherstaette Melcherstaette
Germany Gemeinschaftspraxis Dr. Senftleber, Dr. Kohler Messkirch
Germany Praxisgemeinschaft im Kleinen Biergrund Offenbach/M
Germany Gemeinschaftspraxis Drs. Mockesch Weinheim
Germany Intermed Institud Fur Klinische Forschung und Arzn Wiesbaden
Germany Gemeinschaftspraxis Dr. Emden, Frank Drewes Worpswede
India Apollo Hospital Andhra Pradesh
India Care Hospital Andhra Pradesh
India School of Diabetology, Nizam Institute of Medical Sciences Andhra Pradesh
India Bhagwan Mahaveer Jain Heart Centre Bangalore
India Sri Ramachandra Medical College Hospital Chennai
India Heart Care Clinic Gujarat
India Apollo Hospitals Hyderabaad
India CARE Group of Hospitals Hyderabaad
India St. John's Medical College Hospital Karnataka
India St. John's Medical College Hospital, Karnataka
India Bathia Hospital Maharashtra
India King Edward Medical College & Hospital Maharashtra
India Lokmanya Hospital Maharashtra
India LTMMC & General Hospital Maharashtra
India Ruby Hall Clinic Maharashtra
India Sir J. J. Group of Hospitals Maharashtra
India PD Hinduja Hospital Mumbai
India Apollo Hospital New Delhi
India Sir Gagaram Hospital New Delhi
India Apollo Hospital Tamil Nadu
India Department of Cardiology Tamil Nadu
Israel Department of Internal Medicine, Soroka Medical Center Beersheva
Israel Department of Internal Medicine A, Rambam Medical Center Haifa
Israel Department of Internal Medicine, Wolfson Medical Center Holon
Israel Center for Research, Hadassah University Hospital Jerusalem Ein Kerem
Israel Meir Hospital Kfar Saba
Israel Department of Medicine, Hadassah Medical Center Mount Scopus Jerusalem
Israel Department of Internal Medicine, Rivka Sieff Medical Center Safed
Israel Institute of Metabolic Diseases Tel Aviv
Israel Institute of Lipid & Atherosclerosis Research Tel Hashomer
Italy Dipartimento di Medicina Clinica e Biotecnologia Applicata Bologna
Italy Centro di Ricerca Clinica Chieti
Italy Gerontologia e Geriatria - Universita degli Studi Ferrara
Italy Dipartimento di Medicina Interna DIMI Genova
Italy Universita di Modena e Reggio Emilia, Policlinico Modena
Italy Dipartimento di Medicina Clinica e Sperimentale Napoli
Italy Medicina Clinica e delle Patologie Emergenti Palermo
Italy Dipartimento di Medicina Interna e Scienze Biomediche Parma
Italy U.O Malattie Metaboliche e Diabetologia Treviglio
Italy Azienda Ospedaliero-Universitaria Trieste
Netherlands Andromed Breda Breda
Netherlands Middellaan 5 Breda
Netherlands Andromed Eindhoven Eindhoven
Netherlands Bomanshof 8 Eindhoven
Netherlands Andromed Noord Groningen
Netherlands Damsterdiep 9 Groningen
Netherlands Vasculair Onderzoek Centrum Hoorn Hoorn
Netherlands Andromed Leiden Leiden
Netherlands Doezastraat 1 Leiden
Netherlands Andromed Nijmegen Nijmegen
Netherlands Kamerlingh Onnesstraat 16-18 Nijmegen
Netherlands Andromed Rotterdam Rotterdam
Netherlands Mathenesserlaan 247 Rotterdam
Netherlands Albert Schweitzer Ziekenhuis Sliedrecht
Netherlands Andromed Oost Velp
Netherlands Reigerstraat 30 Velp
Netherlands Rivierenland Tiel Wp Tiel
Netherlands Andromed Zoetermeer Zoetermeer
Netherlands Parkdreef 142 Zoetermeer
Norway Volvat Medisinske Senter Fredrikstad
Norway Nyomen Legekontor Kongsberg
Norway Radhuset Spesialistsenter Oslo
Norway Rikshospitalet - University Hospital Oslo
Norway Skedsmo Medisinske Senter A.S. Skedsmokorset
Poland Podlaski Osrodek Kardiologii Bialystok
Poland NZOZ GCP Dobra Praktyka Lekaska Gruziadz
Poland NZOZ Terapia Optima Katowice
Poland NZOZ Esculap, Przychodnia Lekary Rodzinnych Losice
Poland NZOZ Centrum, Poradnia Kardiologiczna Siedlce
Poland Spec. Gab. Lek. Internistyczno-Kardiologicznly Tarnow
Poland Woj.Szp.Spec.Nr 1 im. Prof. J. Gasinskiego Tychy
Poland Instytut Zywnosci i Zywienia Warszawa
Poland Lecznica PROSEN SMO Warszawa
Poland Szpital Wolski im. Dr A. Gostynskiej Warszawa
Russian Federation Kemerovo Cardiology Dispensary Kemerovo
Russian Federation Central Clinical Hospital 1 of RZD Moscow
Russian Federation City Clinical Hospital 23 Moscow
Russian Federation City Clinical Hospital 64 Moscow
Russian Federation Federal State Institution Out-Patient Clinic 3 of Russian Federation of President’s Management Moscow
Russian Federation Federal State Institution Outpatient Clinic 3 of Russian Federation of President’s Management Moscow
Russian Federation Moscow City Clinical Hospital 68 Moscow
Russian Federation Moscow Regional Research Clinic Institute n.a.M.F.Vladimirov, Department of Therapy Moscow
Russian Federation State Educational Institution of Higher Professional Education “Moscow State University of Medicine and Dentistry of Federal Agency of Health Care and Social Development�, Department of Internal Diseases and Rheumatology based at City Clinica Moscow
Russian Federation State Educational Institution of Higher Professional Education “Moscow State University of Medicine and Dentistry of Federal Agency of Health Care and Social Development�, Hospital Therapy Department # 1 based at City Clinical Hospital # 40 Moscow
Russian Federation State Educational Institution of Higher Professional Education “Moscow State University of Medicine and Dentistry of Federal Agency of Health Care and Social Development�, Hospital Therapy Department #1 based at City Clinical Hospital # 52 Moscow
Russian Federation State Educational Institution of Higher Professional Education “Russian State Medical University Federal Agency of Health Care and Social Development�, Department of Polyclinic Therapy based at Diagnostic Center # 1 Moscow
Russian Federation State Educational Institution of Higher Professional Education “Russian State Medical University Federal Agency of Health Care and Social Development�, Department of Therapy based at City Hospital # 4 Moscow
Russian Federation State Educational Institution of Higher Professional Education “Russian State Medical University of Federal Agency of Health Care and Social Development�, Department of Hospital Therapy #1 based at City Clinical Hospital #15, Cardiology Dept Moscow
Russian Federation State Institution “Research Institute of Physical and Chemical Medicine� of Federal Agency of Health Care and Social Development, Laboratory of Clinical Cardiology based at Bauman City Hospital # 29 Moscow
Russian Federation State Institution “Russian Cardiology Research Complex� of Federal Agency of Health Care and Social Development, Myasnikov Clinical Cardiology Institute, Department of Hemodialysis and Plasmapheresis Moscow
Russian Federation State Research Center for Preventive Medicine Moscow
Russian Federation Novosibirsk Reg. Clinical Cardiology Dispensary Novosibirsk
Russian Federation Central Medical Unit 122, St. Pb Saint Petersburg
Russian Federation Clinical Hospital of Russian Academy of Sciences Saint Petersburg
Russian Federation Consulting and Diagnostic Center 85 Saint Petersburg
Russian Federation Krestovsky Island Medical Institute Saint Petersburg
Russian Federation Pokrovskaya City Hospital Saint Petersburg
Russian Federation St. Petersburg State Medical Institution “Out-patient Clinic # 109� Saint Petersburg
Russian Federation St. Petersburg State Medical Institution “Outpatient Clinic # 109� Saint Petersburg
Russian Federation St. Petersburg State Medical Institution “Pokrovskaya City Hospital�, Cardiology Department #2 Saint Petersburg
Russian Federation State Educational Institution of Higher Professional Education, “Saint-Petersburg State Medical University n.a.Academician I.P.Pavlov of Federal Agency of Health Care and Social Development�, Chair and Department of Faculty Therapy Saint Petersburg
Russian Federation State Educational Institution of Higher Professional Education, “Saint-Petersburg State Medical University n.a.Academician I.P.Pavlov of Federal Agency of Health Care and Social Development�, Institute of Cardiovascular Diseases Saint Petersburg
Spain Hospital de San Vicente Alicante
Spain Hospital Santa Creu I Sant Pau Barcelona
Spain Hospital Santa Creu I Sant Pau, Barcelona
Spain Hospital Universitario de Bellvitge Barcelona
Spain Hospital Vall d'Hebron Barcelona
Spain Hospital Universitario Reina Sofia Cordoba
Spain Centro de Especialidades Pedro Gonzalez Bueno Madrid
Spain Fundacion Jimenez Diaz Madrid
Spain Hospital Clinico San Carlos Madrid
Spain Hospital Ramon y Cajal Madrid
Spain Centro de Salud de Ventanielles Oviedo
Spain Hospital Clinico S. Juan de Alicante San Juan Alicante
Spain Hospital Marques de Valdecilla Santander
Spain Hospital Clinico Universitario de Santiago Santiago de Compostela
Spain Hospital Virgen del Roci-o Sevilla
Spain Hospital Dr. Peset Valencia
Spain Hospital Clinic i Provincial Villaroel Barcelona
Spain Hospital Clinico Lozano Blesa Zaragoza
Spain Hospital Miguel Servet Zaragoza
Sweden Angelholms Sjukhus, Medicinkliniken Angelhom
Sweden Sahlgrenska University Hospital, Intermedicin Gothenburg
Sweden Hjartmottagningen Helsingborg
Sweden Lakarcentrum Nyponet Karineholm
Sweden Medicinkliniken Ludvika
Sweden Huslakaren i Sandviken Sandviken
Sweden Narsjukhuset Sandviken, Kardiologlab, Medicin Sandviken
Sweden Hjart & Karlcenter Sodertalje
Sweden Karolinska Universitetssjukhuset Stockholm
Sweden Hjarthuset AB Varberg
United Kingdom Oldfield Surgery Bath
United Kingdom St James's Surgery Bath
United Kingdom St Michael's Partnership Bath
United Kingdom The Pulteney Practice Bath
United Kingdom Birmingham Clinical Research Centre Birmingham
United Kingdom Stonehill Medical Center Bolton
United Kingdom Avondale Surgery Chesterfield
United Kingdom Chorley Clinical Research Centre Chorley
United Kingdom Saltash Health Center Cornwall
United Kingdom Gomersal Lane Surgery Dronfield
United Kingdom Townhead Research Irvine
United Kingdom Crosby Clinical Research Centre Liverpool
United Kingdom The Symons Medical Center Maidenhead
United Kingdom Manchester Clinical Research Centre Manchester
United Kingdom Greenwood Medical Center Nottingham
United Kingdom Knowle House Surgery Plymouth
United Kingdom Reading Clinical Research Centre Reading
United Kingdom Elm Lane Surgery Sheffield
United Kingdom The Burngreave Surgery Sheffield
United Kingdom Brook Lane Surgery Southampton
United Kingdom St Helier Hospital Surrey
United Kingdom Box Surgery Wiltshire
United Kingdom Bradford Road Medical Center Wiltshire
United Kingdom Eastleigh Surgery Wiltshire
United Kingdom Lovemead Group Practice Wiltshire
United Kingdom Rowden Medical Partnership Wiltshire
United Kingdom St Chad's Surgery Wiltshire
United Kingdom The Health Centre Wiltshire
United Kingdom The Porch Surgery Wiltshire
United Kingdom The Burns Medical Practice Yorkshire

Sponsors (1)

Lead Sponsor Collaborator
Kowa Research Europe

Countries where clinical trial is conducted

Denmark,  Finland,  Germany,  India,  Israel,  Italy,  Netherlands,  Norway,  Poland,  Russian Federation,  Spain,  Sweden,  United Kingdom, 

Outcome

Type Measure Description Time frame Safety issue
Primary Percent Change From Baseline Low Density Lipoprotein-cholesterol (LDL-C) at Week 12 Baseline to 12 weeks No
Secondary Percent Change From Baseline in Total Cholesterol (TC) Baseline to 12 Weeks No
Secondary Percent Change From Baseline in High Density Lipoprotein Cholesterol (HDL-C) Baseline to 12 weeks No
Secondary TC:HDL-C Ratio 12 weeks No
Secondary Triglycerides (TG) 12 weeks No
Secondary Non-HDL:HDL Ratio 12 weeks No
Secondary Apolipoprotein B (Apo B) 12 weeks No
Secondary Apolipoprotein-A1 (Apo-A1) 12 weeks No
Secondary Apo-B:Apo-A1 Ratio 12 weeks No
Secondary High Sensitivity C-reactive Protein (Hs-CRP) at 12 Weeks 12 weeks No
Secondary Oxidized LDL at 12 Weeks 12 weeks No
Secondary National Cholesterol Education Program [NCEP]LDL-C Target Attainment up to 12 weeks No
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