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DyslipidemiaPhase 3NCT00487994

Safety and Efficacy of Lapaquistat Acetate Taken Alone and With Atorvastatin in Subjects With Primary Dyslipidemia

A Phase 3 study testing Lapaquistat acetate, Lapaquistat acetate and atorvastatin and Atorvastatin in people with Dyslipidemia, run by Takeda at 128 sites in 17 countries.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
Search all trials

Trial summary

The purpose of this study is to evaluate the overall safety of Lapaquistat Acetate, once daily (QD), by itself or in combination with atorvastatin in subjects with primary dyslipidemia. Read more about this study

Who is it for?
Ages 18 years and older
Conditions the study is for
Dyslipidemia
What is being tested?
Lapaquistat acetate, Lapaquistat acetate and atorvastatin and Atorvastatin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
2,130 participants
Where
128 sitesin 17 countries
Study dates
Nov 2004to May 2007
Phase
Phase 3
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • Has a confirmatory central laboratory result with low density lipoprotein cholesterol greater than or equal to 3.37 mmol/L and less than 5.69 mmol/L, and triglyceride less than 4.52 mmol/L.
  • Females of child-bearing age must have undergone surgical sterilization, hysterectomy, tubal ligation, or bilateral oophorectomy; other female subjects must have been postmenopausal.
  • Must be in good physical and mental health as determined by a physician on the basis of medical history, physical examination, and laboratory results.
  • Has a fasting low density lipoprotein cholesterol level greater than or equal to 3.37 mmol/L and less than 4.92 mmol/L, and a triglyceride value less than 4.52 mmol/L.

Who cannot join

  • Coronary Heart Disease or Coronary Heart Disease-risk factors comprised of:
  • Diabetes mellitus type 1 or 2.
  • History or presence of myocardial infarction, angina pectoris, unstable angina, coronary angioplasty, coronary or peripheral arterial surgery (bypass graft), aortic aneurysm, transient ischemic attacks, or cerebrovascular accident.
  • A body mass index less than 15 or greater than 35.
  • A history or presence of:
  • Drug abuse or a history of alcohol abuse within the 2 years previous to screening.
Show all 18Show fewer
  • Uncontrolled hypertension despite medical treatment
  • Thyroid disease, particularly hyperthyroidism or subjects whose thyroid replacement therapy was initiated within the previous 3 months.
  • Human immunodeficiency virus-positive status, or hepatitis B or C infection.
  • Malignancy, except subjects whose malignancy had been diagnosed as stage I basal or squamous cell carcinoma.
  • Heterozygous or homozygous familial hypercholesterolemia or known type III hyperlipoproteinemia.
  • Fibromyalgia, myopathy, rhabdomyolysis, or unexplained muscle pain and/or discontinuation of statins due to myalgia.
  • Trauma to the eye or eye irradiation; glaucoma; iritis; uveitis; prior intraocular surgery, laser surgery to the iris, retinal photocoagulation, or laser trabeculoplasty; corneal opacification or other medial opacities; or had undergone LASIK refractive surgery within 6 months prior to screening.
  • A clinically significant food allergy that would prevent adherence to the specialized diet.
  • Any other serious disease or condition that might have affected life expectancy or made it difficult to successfully manage and monitor the subject according to the protocol.
  • Has a known hypersensitivity or history of adverse reaction to atorvastatin or to lapaquistat acetate.
  • Is taking part in another investigational study or had been participating in an investigational study within the 30 days prior to Screening Visit 1.
  • Has an alanine aminotransferase or aspartate aminotransferase level greater than 2 times the upper limit of normal, active liver disease, jaundice, serum creatinine greater than 135 μmol/L (1.5 mg/dL), or creatine kinase greater than 3 times the upper limit of normal.

Trial locations and contacts

128 sites in 17 countries.

128 sites in 17 countries

United States61 sites
  • Study site

    Anaheim, California

  • Study site

    Anderson, South Carolina

  • Study site

    Arlington Heights, Illinois

  • Study site

    Birmingham, Alabama

  • Study site

    Boise, Idaho

  • Study site

    Chandler, Arizona

  • Study site

    Charlotte, North Carolina

  • Study site

    Chicago, Illinois

  • Study site

    Cincinnati, Ohio

  • Study site

    Coral Gables, Florida

  • Study site

    Cordova, Tennessee

  • Study site

    Corpus Christi, Texas

  • Study site

    Dallas, Texas

  • Study site

    Dunwoody, Georgia

  • Study site

    Edina, Minnesota

  • Study site

    Elk Grove Village, Illinois

  • Study site

    Evansville, Indiana

  • Study site

    Flint, Michigan

  • Study site

    Fort Myers, Florida

  • Study site

    Fort Worth, Texas

  • Study site

    Golden, Colorado

  • Study site

    Houston, Texas

  • Study site

    Idaho Falls, Idaho

  • Study site

    Indianapolis, Indiana

  • Study site

    Jacksonville, Florida

  • Study site

    Jonesboro, Arkansas

  • Study site

    Kansas City, Kansas

  • Study site

    Lakewood, Washington

  • Study site

    Little Rock, Arkansas

  • Study site

    Louisville, Kentucky

  • Study site

    Mobile, Alabama

  • Study site

    Morristown, Tennessee

  • Study site

    Mt. Pleasant, South Carolina

  • Study site

    New Orleans, Louisiana

  • Study site

    Norfolk, Virginia

  • Study site

    Northport, Alabama

  • Study site

    Omaha, Nebraska

  • Study site

    Overland Park, Kansas

  • Study site

    Philadelphia, Pennsylvania

  • Study site

    Phoenix, Arizona

  • Study site

    Plano, Texas

  • Study site

    Rancho Cucamonga, California

  • Study site

    Richmond, Virginia

  • Study site

    Rochester, New York

  • Study site

    San Antonio, Texas

  • Study site

    Santa Rosa, California

  • Study site

    Sarasota, Florida

  • Study site

    Ship Bottom, New Jersey

  • Study site

    Sierra Vista, Arizona

  • Study site

    Simpsonville, South Carolina

  • Study site

    St Louis, Missouri

  • Study site

    Statesville, North Carolina

  • Study site

    Syracuse, New York

  • Study site

    Temple, Texas

  • Study site

    Texarkana, Texas

  • Study site

    Tipton, Pennsylvania

  • Study site

    Tulsa, Oklahoma

  • Study site

    Waterloo, Iowa

  • Study site

    West Palm Beach, Florida

  • Study site

    Wilmington, North Carolina

  • Study site

    Winston-Salem, North Carolina

Other trials in United States

Poland9 sites
  • Study site

    Bialystok

  • Study site

    Bydgoszcz

  • Study site

    Gdansk

  • Study site

    Gorzów Wielkopolski

  • Study site

    Grudziądz

  • Study site

    Płońsk

  • Study site

    Torun

  • Study site

    Włocławek

  • Study site

    Wroclaw

Other trials in Poland

Argentina8 sites
  • Study site

    Buenos Aires

  • Study site

    Córdoba

  • Study site

    La Plata

  • Study site

    Morón

  • Study site

    Pilar

  • Study site

    Rosario

  • Study site

    Salta

  • Study site

    Santa Fe

Other trials in Argentina

Germany8 sites
  • Study site

    Berlin

  • Study site

    Freiburg im Breisgau

  • Study site

    Görlitz

  • Study site

    Hamburg

  • Study site

    Mannheim

  • Study site

    Mönchengladbach

  • Study site

    Munich

  • Study site

    Schwerin

Other trials in Germany

Hungary7 sites
  • Study site

    Budapest

  • Study site

    Debrecen

  • Study site

    Esztergom

  • Study site

    Győr

  • Study site

    Gyula

  • Study site

    Kecskemét

  • Study site

    Warszawa

Other trials in Hungary

Mexico6 sites
  • Study site

    Distrito Federal

  • Study site

    Guadalajara

  • Study site

    Jalisco

  • Study site

    Mexico City

  • Study site

    San Luis Potosí City

  • Study site

    Zapopan

Other trials in Mexico

Netherlands5 sites
  • Study site

    Es Velp

  • Study site

    Groningen

  • Study site

    Leiden

  • Study site

    Rotterdam

  • Study site

    Zoetermeer

Other trials in Netherlands

South Africa4 sites
  • Study site

    Cape Town

  • Study site

    Johannesburg

  • Study site

    Parow

  • Study site

    Western Cape

Other trials in South Africa

United Kingdom4 sites
  • Study site

    Blackpool, Lancashire

  • Study site

    Bolton, Lancashire

  • Study site

    Guildford, Surrey

  • Study site

    Truro, Cornwall

Other trials in United Kingdom

Czechia3 sites
  • Study site

    Brno

  • Study site

    Olomouc

  • Study site

    Prague

Other trials in Czechia

Lithuania3 sites
  • Study site

    Kaunas

  • Study site

    Vilnius

  • Study site

    Vilnius-21

Other trials in Lithuania

Russia3 sites
  • Study site

    Moscow

  • Study site

    Saint Petersburg

  • Study site

    Saratov

Other trials in Russia

Slovakia3 sites
  • Study site

    Komárno

  • Study site

    Košice

  • Study site

    Levice

Other trials in Slovakia

Chile1 site
  • Study site

    Santiago

Other trials in Chile

Estonia1 site
  • Study site

    Tartu

Other trials in Estonia

Latvia1 site
  • Study site

    Riga

Other trials in Latvia

Peru1 site
  • Study site

    Lima

Other trials in Peru

About this study

Official title: A Double-Blind, Randomized, Parallel Group Study to Evaluate the Safety, Tolerability and Efficacy of Lapaquistat Acetate Alone or Coadministered With Atorvastatin in Subjects With Primary Dyslipidemia

The purpose of this study is to evaluate the overall safety of Lapaquistat Acetate, once daily (QD), by itself or in combination with atorvastatin in subjects with primary dyslipidemia.

Read the detailed description

According to the World Health Organization, CHD is now the leading cause of death worldwide. In 2001, CHD caused 7.2 million deaths and estimates for 2020 indicate that annual CHD deaths will increase to 11.1 million. These statistics suggest that improved options are needed to treat hypercholesterolemia and dyslipidemia.

The balance among cholesterol synthesis, dietary intake, and degradation is normally adequate to maintain healthy cholesterol plasma levels. However, in patients with hypercholesterolemia, elevated low-density lipoprotein cholesterol leads to atherosclerotic deposition of cholesterol in the arterial walls. Consequently, in this population it has been established that lowering low-density lipoprotein cholesterol plasma concentrations effectively reduces cardiovascular morbidity and mortality. The National Cholesterol Education Program Adult Treatment Panel III has therefore identified control of low-density lipoprotein cholesterol as essential in the prevention and management of CHD. Additional lipid risk factors designated by National Cholesterol Education Program Adult Treatment Panel III include elevated triglycerides, elevated non-high-density lipoprotein cholesterol (atherogenic lipoproteins), and low levels of high-density lipoprotein cholesterol. Lipoproteins rich in triglycerides, such as very-low-density lipoprotein cholesterol, appear to contribute to atherosclerosis, whereas the apparent protective effect of high-density lipoprotein cholesterol, which is likely related to high-density lipoprotein cholesterol-facilitated transport of cholesterol away from atherosclerotic deposits, may be limited at low high-density lipoprotein cholesterol concentrations.

Initial dietary and lifestyle measures taken to control dyslipidemia are often inadequate, and most patients require pharmacologic intervention. Currently, 3-hydroxy-3-methylglutaryl coenzyme A reductase inhibitors (statins) are the first-line monotherapies most often prescribed to reduce low-density lipoprotein cholesterol, after diet and therapeutic lifestyle change. However, with statin monotherapy, many patients fail to reach National Cholesterol Education Program Adult Treatment Panel III recommended levels of low-density lipoprotein cholesterol reduction. As a result, the statin dosage must be increased or an additional treatment added to achieve treatment goals. Increasing the statin dosage may result in decreased tolerability and potential safety concerns, contributing to the high discontinuation rates of statins and their prescription at low and often ineffective doses. Further, although the effectiveness of increasing the dose varies among the statins, in general, doubling of the dose above the minimum effective dose has been found to decrease serum low-density lipoprotein cholesterol by only an additional 6 percent.

TGRD is developing an orally active squalene synthase inhibitor, TAK-475 (lapaquistat acetate) for the treatment of dyslipidemia. Lapaquistat acetate inhibits the biosynthesis of cholesterol by inhibiting the enzyme squalene synthase, which catalyzes the conversion of farnesyl diphosphate to squalene-a precursor in the final steps of cholesterol production.

Study Participation is anticipated to be up to two years.

Conditions
Dyslipidemia
Being tested
Lapaquistat acetate, Lapaquistat acetate and atorvastatin, Atorvastatin
Keywords
Hypercholesterolemia, Hyperlipidemia, Drug Therapy
Medical subject headings
Dyslipidemias, Hypercholesterolemia, Hyperlipidemias

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Lapaquistat acetateDrug

    Also called TAK-475

    Lapaquistat acetate 100 mg, tablets, orally, once daily and Atorvastatin placebo-matching capsules, orally, once daily for up to 96 weeks.

  • Lapaquistat acetate and atorvastatinDrug

    Also called TAK-475, Lipitor

    Lapaquistat acetate 100 mg, tablets, orally, once daily and Atorvastatin 10 mg, capsules, orally, once daily for up to 96 weeks.

  • AtorvastatinDrug

    Also called Lipitor

    Lapaquistat acetate placebo-matching tablets, orally, once daily and Atorvastatin 10 mg, capsules, orally, once daily for up to 96 weeks.

Study groups in NCT00487994
Study groupRoleWhat they receive
Lapaquistat Acetate 100 mg QDExperimentalNot described
Receives: Drug: Lapaquistat acetate
Lapaquistat Acetate 100 mg QD + Atorvastatin 10 mg QDExperimentalNot described
Receives: Drug: Lapaquistat acetate and atorvastatin
Atorvastatin 10 mg QDActive comparatorNot described
Receives: Drug: Atorvastatin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Lens Opacity Classification System findings

    Measured: Weeks 24, 48, 72, and 96 or Final Visit

  2. Best corrected visual acuity

    Measured: Weeks 24, 48, 72, and 96 or Final Visit

  3. Adverse Events

    Measured: Weeks 4, 8, 12, 24, 36, 48, 60, 72, 84, 96 or Final Visit

  4. Clinical Laboratory Tests

    Measured: Weeks 4, 8, 12, 24, 36, 48, 60, 72, 84, 96 or Final Visit

  5. Vital signs (blood pressure and pulse rate) and weight

    Measured: Weeks 4, 8, 12, 24, 36, 48, 60, 72, 84, 96 or Final Visit

  6. 12-lead Electrocardiogram

    Measured: Weeks 48 and 96 or Final Visit

  7. Physical Examination

    Measured: Weeks 48 and 96 or Final Visit

Secondary outcomes (7)
  1. Change from Baseline in Low Density Lipoprotein cholesterol

    Measured: Week 96 or Final Visit

  2. Change from Baseline in High Density Lipoprotein cholesterol

    Measured: Week 96 or Final Visit

  3. Change from Baseline in Total Cholesterol

    Measured: Week 96 or Final Visit

  4. Change from Baseline in Triglycerides

    Measured: Week 96 or Final Visit

  5. Change from Baseline in Very Low Density Lipoprotein cholesterol

    Measured: Week 96 or Final Visit

  6. Change from Baseline in Apolipoprotein A1

    Measured: Week 96 or Final Visit

  7. Change from Baseline in Apolipoprotein B

    Measured: Week 96 or Final Visit

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted19 Jun 2007 (estimated)
  2. Study startNov 2004
  3. Primary completionMay 2007
  4. Study completionMay 2007

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 3
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Quadruple blind
Who is masked
Participant, Care provider, Investigator, Outcomes assessor
Enrolment
2,130 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT00487994
Sponsor's protocol ID
01-04-TL-475-002
Other IDs
2004-000775-34, U1111-1122-7619, 2004
Status last verified
May 2012
First submitted
15 Jun 2007
Last updated
24 May 2012
Results posted
No
Data monitoring committee
Yes

Publications

  • Stein EA, Bays H, O'Brien D, Pedicano J, Piper E, Spezzi A. Lapaquistat acetate: development of a squalene synthase inhibitor for the treatment of hypercholesterolemia. Circulation. 2011 May 10;123(18):1974-85. doi: 10.1161/CIRCULATIONAHA.110.975284. Epub 2011 Apr 25.

    PubMed 21518985

Questions about this trial

What is this clinical trial studying?

A Phase 3 study testing Lapaquistat acetate, Lapaquistat acetate and atorvastatin and Atorvastatin in people with Dyslipidemia, run by Takeda at 128 sites in 17 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 4 inclusion and 18 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 24 May 2012. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 128 sites in United States, Poland, Argentina, Germany, Hungary and 12 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Lens Opacity Classification System findings (time frame: Weeks 24, 48, 72, and 96 or Final Visit). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?

On the ClinicalTrials.gov record for NCT00487994, which also lists 1 linked publication.

Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 May 2012.

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