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Terminated Phase 3 Interventional

Study To Evaluate The Effect Of Torcetrapib/Atorvastatin In Subjects With A Genetic Cholesterol Disorder.

ClinicalTrials.gov ID: NCT00145431

Public ClinicalTrials.gov record NCT00145431. 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 May 10, 2026, 10:31 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

Phase 3, Multi-Center, Double-Blind, Randomized, Crossover Study Of The Efficacy, Safety, And Tolerability Of Fixed Combination Torcetrapib (Cp-529,414)/Atorvastatin, Compared With Atorvastatin Therapy Alone, And Fenofibrate Alone, In Subjects With Fredrickson Type III Hyperlipoproteinemia (Familial Dysbetalipoproteinemia).

Study identification

NCT ID
NCT00145431
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
41 participants

Conditions and interventions

Interventions

  • atorvastatin Drug
  • fenofibrate Drug
  • torcetrapib/atorvastatin Drug

Drug

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
Feb 28, 2005
Primary completion
Nov 30, 2006
Completion
Nov 30, 2006
Last update posted
Feb 16, 2012

2005 – 2006

United States locations

U.S. sites
22
U.S. states
13
U.S. cities
21
Facility City State ZIP Site status
Pfizer Investigational Site Anaheim California 92804
Pfizer Investigational Site Huntington Beach California 92648
Pfizer Investigational Site Orange California 92868
Pfizer Investigational Site Pacific Palisades California 90272
Pfizer Investigational Site Studio City California 91604
Pfizer Investigational Site Tustin California 92780
Pfizer Investigational Site Hollywood Florida 33021
Pfizer Investigational Site Longwood Florida 32779
Pfizer Investigational Site Tripler Army Medical Center Hawaii 96859-5000
Pfizer Investigational Site Scarborough Maine 04074
Pfizer Investigational Site Portage Michigan 49002
Pfizer Investigational Site Portage Michigan 49024
Pfizer Investigational Site Olive Branch Mississippi 38654
Pfizer Investigational Site Rochester New York 14618
Pfizer Investigational Site Syracuse New York 13210
Pfizer Investigational Site West Seneca New York 14224
Pfizer Investigational Site Sellersville Pennsylvania 18960
Pfizer Investigational Site Greer South Carolina 29651
Pfizer Investigational Site Memphis Tennessee 38105
Pfizer Investigational Site Salt Lake City Utah 84108
Pfizer Investigational Site Seattle Washington 98104
Pfizer Investigational Site Madison Wisconsin 53719

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 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00145431, 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 Feb 16, 2012 · Synced May 10, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00145431 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →