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Completed Phase 2 Interventional

Effect of Lapaquistat Acetate Combined With Fenofibrate on Blood Cholesterol Levels

ClinicalTrials.gov ID: NCT00813527

Public ClinicalTrials.gov record NCT00813527. 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 Sep 5, 2026, 5:13 PM 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 TAK-475 or Placebo When Coadministered With Fenofibrate in Subjects With Combined Hyperlipidemia

Brief summary

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

The purpose of this study is to compare changes in cholesterol levels in patients with elevated blood cholesterol with administration of lapaquistat acetate, once daily (QD), and fenofibrate.

Study identification

NCT ID
NCT00813527
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Takeda
Industry
Enrollment
213 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
Jan 31, 2006
Primary completion
Dec 31, 2006
Completion
Dec 31, 2006
Last update posted
May 23, 2012

2006 – 2007

United States locations

U.S. sites
32
U.S. states
19
U.S. cities
32
Facility City State ZIP Site status
Not listed Huntsville Alabama
Not listed Sierra Vista Arizona
Not listed Beverly Hills California
Not listed Long Beach California
Not listed Spring Valley California
Not listed Colorado Springs Colorado
Not listed Golden Colorado
Not listed Waterbury Connecticut
Not listed Jacksonville Florida
Not listed Kissimmee Florida
Not listed Miami Florida
Not listed Ocala Florida
Not listed Pembroke Pines Florida
Not listed Pinellas Park Florida
Not listed West Palm Beach Florida
Not listed Warner Robins Georgia
Not listed Chicago Illinois
Not listed Peoria Illinois
Not listed Indianapolis Indiana
Not listed Wichita Kansas
Not listed Edina Minnesota
Not listed St Louis Missouri
Not listed Raleigh North Carolina
Not listed Winston-Salem North Carolina
Not listed Cincinnati Ohio
Not listed Columbus Ohio
Not listed Hillsboro Oregon
Not listed Beaver Pennsylvania
Not listed Goose Creek South Carolina
Not listed Nashville Tennessee
Not listed Norfolk Virginia
Not listed Richmond Virginia

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 4 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00813527, 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 23, 2012 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00813527 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →