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ClinicalTrials.gov record
Completed Phase 3 Interventional

Lipitor Trial To Study The Effect Of Torcetrpib/Atorvastatin To Atorvastatin Alone.

ClinicalTrials.gov ID: NCT00137462

Public ClinicalTrials.gov record NCT00137462. 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 30, 2026, 9:53 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 Phase 3, Double-Blind, Randomized, Multisite Trial Of The Efficacy, Safety, And Tolerability Of The Fixed Combination Torcetrapib/Atorvastatin Administered Orally, Once Daily For 12 Months, Compared To Atorvastatin Alone, Titrated Based On NCEP ATP-III LDL-C Goals In Subjects With Fredrickson Types IIa And IIb Dyslipidemias

Brief summary

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

The Torcetrapib project was terminated on December 2, 2006 due to safety findings. To look at various lipids in the blood of people with Fredrickson Type IIa and Type IIb mixed dyslipidemias

Study identification

NCT ID
NCT00137462
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
900 participants

Conditions and interventions

Conditions

Interventions

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
Nov 2004 (Type not available)
Primary completion
Not listed
Completion
Sep 2006 (Type not available)
Last update posted
Nov 16, 2007

2004 – 2006

United States locations

U.S. sites
48
U.S. states
20
U.S. cities
43
Facility City State ZIP Site status
Pfizer Investigational Site Huntsville Alabama 35802 —
Pfizer Investigational Site Union Grove Alabama 35175 —
Pfizer Investigational Site Fresno California 93720 —
Pfizer Investigational Site Los Angeles California 90057 —
Pfizer Investigational Site Orange California 92868 —
Pfizer Investigational Site San Diego California 92128 —
Pfizer Investigational Site Denver Colorado 80220 —
Pfizer Investigational Site Denver Colorado 80262 —
Pfizer Investigational Site Golden Colorado 80401 —
Pfizer Investigational Site Bridgeport Connecticut 06610 —
Pfizer Investigational Site Fairfield Connecticut 06824 —
Pfizer Investigational Site Trumbull Connecticut 06611 —
Pfizer Investigational Site Waterbury Connecticut 06708 —
Pfizer Investigational Site Washington D.C. District of Columbia 20037 —
Pfizer Investigational Site Boynton Beach Florida 33437 —
Pfizer Investigational Site Fort Lauderdale Florida 33308 —
Pfizer Investigational Site Gainesville Florida 32605 —
Pfizer Investigational Site Gainesville Florida 32610 —
Pfizer Investigational Site Gainsville Florida 32610 —
Pfizer Investigational Site Sebastian Florida 32958 —
Pfizer Investigational Site Vero Beach Florida 32960 —
Pfizer Investigational Site Rockford Illinois 61108 —
Pfizer Investigational Site Springfield Illinois 62704 —
Pfizer Investigational Site Olathe Kansas 66061 —
Pfizer Investigational Site Overland Park Kansas 66210 —
Pfizer Investigational Site Madisonville Kentucky 42431 —
Pfizer Investigational Site Burlington Massachusetts 01805 —
Pfizer Investigational Site Grand Rapids Michigan 49525 —
Pfizer Investigational Site Troy Michigan 48098 —
Pfizer Investigational Site Albuquerque New Mexico 87102 —
Pfizer Investigational Site Albuquerque New Mexico 87106 —
Pfizer Investigational Site Orchard Park New York 14127 —
Pfizer Investigational Site Syracuse New York 13202 —
Pfizer Investigational Site Syracuse New York 13210 —
Pfizer Investigational Site Williamsville New York 14221 —
Pfizer Investigational Site Charlotte North Carolina 28262 —
Pfizer Investigational Site Cleveland Ohio 44126 —
Pfizer Investigational Site Columbus Ohio 43214 —
Pfizer Investigational Site Keizer Oregon 97303 —
Pfizer Investigational Site Salem Oregon 97302 —
Pfizer Investigational Site Doylestown Pennsylvania 18901 —
Pfizer Investigational Site Charleston South Carolina 29425 —
Pfizer Investigational Site Mt. Pleasant South Carolina 29464 —
Pfizer Investigational Site Mt. Pleasant South Carolina 83464 —
Pfizer Investigational Site Kingsport Tennessee 37660 —
Pfizer Investigational Site Morristown Tennessee 37813 —
Pfizer Investigational Site Dallas Texas 75230 —
Pfizer Investigational Site McKinney Texas 75069 —

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 11 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00137462, 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 Nov 16, 2007 · Synced Oct 30, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00137462 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →