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临床试验/NCT00137462
NCT00137462已完成3 期

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

Pfizer60 个研究点 分布在 2 个国家目标入组 900 人开始时间: 2004年11月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
已完成
发起方
Pfizer
入组人数
900
试验地点
60
主要终点
Change in lipid parameters (HDL, LDL) at various timepoints over 12 months.

研究概览

简要总结

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

详细描述

For additional information please call: 1-800-718-1021

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Statin eligible per NCEP ATP-III guidelines
  • At least 18 years of age

排除标准

  • Women who are pregnant or lactating, or planning to become pregnant
  • Intolerance to statin therapy
  • Subjects taking any drugs known to be associated with an increased risk of myositis in combination with HMG-CoA reductase inhibitors
  • Subjects with any other medical condition or laboratory abnormality which could affect subject safety, preclude evaluation of response, or render unlikely that the subject would complete the study

结局指标

主要结局

Change in lipid parameters (HDL, LDL) at various timepoints over 12 months.

次要结局

  • Changes in levels of lipids and other biomarkers.

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (60)

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