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Sponsored by: |
Pfizer |
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Information provided by: | Pfizer |
ClinicalTrials.gov Identifier: | NCT00139061 |
The Torcetrapib project was terminated on December 2, 2006 due to safety findings.
To assess the HDL-C increase and non-HDL lowering effect of torcetrapib/atorvastatin vs. fenofibrate.
Condition | Intervention | Phase |
---|---|---|
Hyperlipidemia |
Drug: Torcetrapib/Atorvastatin Drug: Fenofibrate |
Phase III |
Study Type: | Interventional |
Study Design: | Treatment, Randomized, Double-Blind, Active Control, Parallel Assignment, Safety/Efficacy Study |
Official Title: | Phase 3 Multi-Center, Double-Blind, Randomized, Parallel Group, Forced Titration Study Of The Efficacy, Safety, And Tolerability Of Torcetrapib/Atorvastatin Compared To Fenofibrate In Subjects With Fredrickson Type IIB Dyslipidemia (Mixed Hyperlipidemia |
Estimated Enrollment: | 128 |
Study Start Date: | March 2005 |
Estimated Study Completion Date: | May 2006 |
For additional information please call: 1-800-718-1021
Ages Eligible for Study: | 18 Years and older |
Genders Eligible for Study: | Both |
Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
France | |
Pfizer Investigational Site | |
Dijon, France, 21000 | |
Pfizer Investigational Site | |
Thouars, France, 79100 | |
Pfizer Investigational Site | |
Briollay, France, 49125 | |
Pfizer Investigational Site | |
Saint Martin D'Oney, France, 40090 | |
Pfizer Investigational Site | |
Mont de Marsan, France, 40000 | |
Pfizer Investigational Site | |
Strasbourg, France, 67000 | |
Pfizer Investigational Site | |
Jarny, France, 54800 | |
Pfizer Investigational Site | |
Metz, France, 57070 | |
Pfizer Investigational Site | |
Moutiers, France, 54660 | |
Pfizer Investigational Site | |
Bordeaux Cauderan, France, 33 200 | |
Pfizer Investigational Site | |
Tierce, France, 49 125 | |
Pfizer Investigational Site | |
Angers, France, 49 100 | |
Pfizer Investigational Site | |
Angers, France, 49 000 | |
Pfizer Investigational Site | |
Hagondange, France, 57 300 | |
Pfizer Investigational Site | |
Pouilly en Auxois, France, 21 850 | |
Pfizer Investigational Site | |
Nantes, France, 44 093 Cedex 01 | |
Pfizer Investigational Site | |
Mont de Marsan, France, 40 010 cedex | |
Pfizer Investigational Site | |
Mont de Marsan CEDEX, France, 40010 | |
Pfizer Investigational Site | |
Mont de Marsan, France, 40 010 | |
Pfizer Investigational Site | |
Monguilhem, France, 32 240 | |
Pfizer Investigational Site | |
Saint Justin, France, 40 240 | |
Pfizer Investigational Site | |
Haut Mauco, France, 40 280 | |
Pfizer Investigational Site | |
Lille, France, 59 037 Cedex | |
Pfizer Investigational Site | |
Murs Erigne, France, 49610 | |
Pfizer Investigational Site | |
Mars LA Tour, France, 54800 | |
Pfizer Investigational Site | |
Seysses, France, 31600 |
Study Director: | Pfizer CT.gov Call Center | Pfizer |
Study ID Numbers: | A5091034 |
Study First Received: | August 26, 2005 |
Last Updated: | October 30, 2007 |
ClinicalTrials.gov Identifier: | NCT00139061 |
Health Authority: | United States: Food and Drug Administration |
Metabolic Diseases Hyperlipidemias Torcetrapib Hyperlipidemia, Familial Combined Metabolic disorder |
Procetofen Combined hyperlipidemia, familial Atorvastatin Dyslipidemias Lipid Metabolism Disorders |
Antimetabolites Molecular Mechanisms of Pharmacological Action Therapeutic Uses Antilipemic Agents |
Enzyme Inhibitors Anticholesteremic Agents Hydroxymethylglutaryl-CoA Reductase Inhibitors Pharmacologic Actions |