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Completed Phase 3 Interventional

A Study Comparing The Efficacy & Safety Of Torcetrapib/Atorvastatin And Atorvastatin In Subjects With High Triglycerides

ClinicalTrials.gov ID: NCT00134498

Public ClinicalTrials.gov record NCT00134498. 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 29, 2026, 8:54 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-Site, Double-Blind, Randomized, Forced Titration, Parallel Group Evaluation Of The Efficacy, Safety, And Tolerability Of Fixed Combination Torcetrapib (CP 529,414)/Atorvastatin Administered Orally, Once Daily (Qd) For Eighteen Weeks, Compared With Atorvastatin Alone, In Subjects With Fredrickson Type IV Hypertriglyceridemia

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 assess the safety and efficacy of the fixed combination torcetrapib/atorvastatin in subjects with Fredrickson Type IV Hypertriglyceridemia.

Study identification

NCT ID
NCT00134498
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Pfizer
Industry
Enrollment
160 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
Feb 2005 (Type not available)
Primary completion
Not listed
Completion
Nov 2006 (Type not available)
Last update posted
Nov 16, 2007

2005 – 2006

United States locations

U.S. sites
39
U.S. states
23
U.S. cities
39
Facility City State ZIP Site status
Pfizer Investigational Site Anaheim California — —
Pfizer Investigational Site Huntington Beach California — —
Pfizer Investigational Site Los Angeles California — —
Pfizer Investigational Site Orange California — —
Pfizer Investigational Site Orangevale California — —
Pfizer Investigational Site Pacific Palisades California — —
Pfizer Investigational Site Studio City California — —
Pfizer Investigational Site Tustin California — —
Pfizer Investigational Site Walnut Creek California — —
Pfizer Investigational Site Farmington Connecticut — —
Pfizer Investigational Site Washington D.C. District of Columbia — —
Pfizer Investigational Site Hollywood Florida — —
Pfizer Investigational Site Longwood Florida — —
Pfizer Investigational Site West Palm Beach Florida — —
Pfizer Investigational Site Tripler AMC Hawaii — —
Pfizer Investigational Site Chicago Illinois — —
Pfizer Investigational Site Indianapolis Indiana — —
Pfizer Investigational Site Overland Park Kansas — —
Pfizer Investigational Site Baton Rouge Louisiana — —
Pfizer Investigational Site Scarborough Maine — —
Pfizer Investigational Site Bethesda Maryland — —
Pfizer Investigational Site Ann Arbor Michigan — —
Pfizer Investigational Site Canton Michigan — —
Pfizer Investigational Site Portage Michigan — —
Pfizer Investigational Site Richland Michigan — —
Pfizer Investigational Site Saint Cloud Minnesota — —
Pfizer Investigational Site Olive Branch Mississippi — —
Pfizer Investigational Site Jefferson City Missouri — —
Pfizer Investigational Site St Louis Missouri — —
Pfizer Investigational Site Las Vegas Nevada — —
Pfizer Investigational Site Rochester New York — —
Pfizer Investigational Site Syracuse New York — —
Pfizer Investigational Site West Seneca New York — —
Pfizer Investigational Site Statesville North Carolina — —
Pfizer Investigational Site Sellersville Pennsylvania — —
Pfizer Investigational Site Warwick Rhode Island — —
Pfizer Investigational Site San Antonio Texas — —
Pfizer Investigational Site Richmond Virginia — —
Pfizer Investigational Site Madison Wisconsin — —

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 NCT00134498, 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 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00134498 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →