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临床试验/NCT00697203
NCT00697203已完成2 期

A Randomized, Double-blind Study of the Effect of RO4607381 in Combination With Pravastatin on HDL-cholesterol (HDL-C) Levels in Patients With Low or Average HDL-C Levels

Hoffmann-La Roche0 个研究点目标入组 292 人开始时间: 2005年7月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
292
主要终点
Percent Change From Baseline in HDL-C Level\n

研究概览

简要总结

This 4 arm study will evaluate the efficacy and safety of RO4607381 when co-administered with pravastatin in patients with low or relatively low HDL-C levels. Patients will be randomised to one of 4 groups to receive either RO4607381 300mg, 600mg or 900mg po daily, or placebo po daily, for 12 weeks.All patients will also receive pravastatin 40mg po daily for 12 weeks.The anticipated time on study treatment is 3 months and the target sample size is 100-500 individuals.

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 (Participant, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • adult patients 18-75 years of age;
  • dyslipidemic patients with low or relatively low HDL-C levels during treatment with pravastatin.

排除标准

  • women who are pregnant, breastfeeding, or of child-bearing potential;
  • morbid obesity;
  • uncontrolled hypertension;
  • poorly controlled or insulin-treated diabetes;
  • high creatinine levels or history of statin-associated myopathy.

研究组 & 干预措施

Placebo

Placebo Comparator

干预措施: Pravastatin (Drug)

Dalcetrapib 300mg

Experimental

干预措施: Pravastatin (Drug)

Dalcetrapib 300mg

Experimental

干预措施: Dalcetrapib (Drug)

Dalcetrapib 600mg

Experimental

干预措施: Pravastatin (Drug)

Dalcetrapib 600mg

Experimental

干预措施: Dalcetrapib (Drug)

Dalcetrapib 900mg

Experimental

干预措施: Pravastatin (Drug)

Dalcetrapib 900mg

Experimental

干预措施: Dalcetrapib (Drug)

Placebo

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Percent Change From Baseline in HDL-C Level\n

时间窗: 12 Weeks

Absolute Change From Baseline in HDL-C Level\n

时间窗: Week 12

次要结局

  • Ratios of Total HDL-C/LDL-C, HDL-2/HDL-3, ApoA1/ApoB(Baseline and at 12 Weeks)
  • AEs, Lab Parameters, Vital Signs, ECG(Through 9 Months)
  • Percent Change of Fasting Glucose Level(12 weeks)
  • Change From Baseline in: Total Cholesterol, Triglycerides, HDL-C, LDL-C, HDL-2, HDL-3, ApoA1, ApoA2, ApoB, LpAI(12 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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