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临床试验/NCT01133210
NCT01133210已完成1 期

Effect of Maraviroc on Metabolic Function in Obese Subjects (Phase I)

Washington University School of Medicine1 个研究点 分布在 1 个国家目标入组 27 人开始时间: 2011年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
27
试验地点
1
主要终点
effect of Maraviroc on plasma triglyceride concentration

研究概览

简要总结

The purpose of this study is to determine the effect of maraviroc therapy in obese insulin resistant subjects on:

  1. Plasma triglyceride concentration
  2. Plasma HDL-cholesterol and LDL-cholesterol concentrations
  3. Plasma markers of cardiometabolic risk and inflammation

详细描述

The purpose of this study is to determine, in obese insulin resistant subjects, the effect of maraviroc therapy, a selective antagonist of the human chemokine receptor CCR5, on:

  1. Plasma triglyceride concentration
  2. Plasma HDL-cholesterol and LDL-cholesterol concentrations
  3. Plasma markers of cardiometabolic risk and inflammation

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
Single (Participant)

入排标准

年龄范围
18 Years 至 64 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • obese (body mass index (BMI) between 30 and 45.9)
  • increased plasma triglyceride concentrations (150-400 mg/dL)

排除标准

  • active or previous infection with hepatitis B or C
  • history of alcohol abuse
  • current alcohol consumption (>20g/day)
  • severe hypertriglyceridemia (>400 mg/dL)
  • active peptic ulcer disease
  • pregnant or lactating
  • take statins, fibrates, niacin, moderate to strong Cyp3A4 inhibitors or inducers, or any other medication that might confound interpretation of the study results will be excluded.

研究组 & 干预措施

Maraviroc

Experimental

Subjects will receive 12 weeks of treatment with maraviroc (300 mg po bid).

干预措施: Maraviroc (Drug)

Placebo

Placebo Comparator

Subjects will receive 12 weeks of treatment with placebo

干预措施: placebo (Other)

结局指标

主要结局

effect of Maraviroc on plasma triglyceride concentration

时间窗: 12 weeks

We will compare pre and post-treatment serum triglyceride concentrations in subjects receiving a 12 week course of either Maraviroc or placebo.

次要结局

  • Effect of Maraviroc on serum HDL concentration(12 weeks)
  • Effect of Maraviroc on plasma markers of cardiometabolic risk and inflammation(12 weeks)
  • effect of Maraviroc on serum LDL-cholesterol concentration(12 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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