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Completed Phase 3 Interventional

Efficacy of Lapaquistat Acetate Alone or Combined With Rosuvastatin in Subjects With Hypercholesterolemia

ClinicalTrials.gov ID: NCT00249912

Public ClinicalTrials.gov record NCT00249912. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 17, 2026, 6:50 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Double-Blind, Randomized Study to Evaluate the Efficacy and Safety of Lapaquistat Acetate 50 mg, 100 mg or Placebo When Coadministered With Rosuvastatin 10 mg or 20 mg in Subjects With Primary Hypercholesterolemia

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate lapaquistat acetate, once daily (QD), taken alone or with rosuvastatin on cholesterol levels in treating patients with elevated cholesterol.

Study identification

NCT ID
NCT00249912
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Takeda
Industry
Enrollment
415 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2005 (Type not available)
Primary completion
Apr 2007 (Actual)
Completion
Apr 2007 (Actual)
Last update posted
May 24, 2012

2005 – 2007

United States locations

U.S. sites
82
U.S. states
32
U.S. cities
82
Facility City State ZIP Site status
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Not listed Concord New Hampshire — —
Not listed West Seneca New York — —
Not listed Raleigh North Carolina — —
Not listed Statesville North Carolina — —
Not listed Winstom-Salem North Carolina — —
Not listed Grand Forks North Dakota — —
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Not listed Scotland Pennsylvania — —
Not listed Cranston Rhode Island — —
Not listed Anderson South Carolina — —
Not listed Bristol Tennessee — —
Not listed Cordova Tennessee — —
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Not listed Salt Lake City Utah — —
Not listed Burke Virginia — —
Not listed Norfolk Virginia — —
Not listed Richmond Virginia — —
Not listed Weber City Virginia — —
Not listed Bellevue Washington — —
Not listed Burien Washington — —
Not listed Edmonds Washington — —
Not listed Seattle Washington — —
Not listed Spokane Washington — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 10 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00249912, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted May 24, 2012 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00249912 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →