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临床试验/NCT00131391
NCT00131391终止3 期

A 2-Year Study (1-Year Weight Loss Followed by 1-Year Prevention of Weight Regain) to Assess the Safety, Tolerability and Efficacy of Taranabant (MK0364) in Obese Patients Followed by a 1-Year Extension

Merck Sharp & Dohme LLC0 个研究点目标入组 2,400 人开始时间: 2005年7月最近更新:
适应症
相关药物

试验速览

阶段
3 期
状态
终止
入组人数
2,400
主要终点
Decreases body weight; prevention of weight regain; safety and tolerability

研究概览

简要总结

A worldwide study in obese patients to assess the efficacy, safety, and tolerability of an investigational drug.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Body Mass Index (BMI) between 30-43 kg/m2

排除标准

  • History of major psychiatric disorder
  • History of seizures or at high risk of developing seizures
  • Blood pressure greater than 160/100
  • Fasting blood glucose greater than 126 mg/dL
  • Triglycerides greater than 600 mg/dL

结局指标

主要结局

Decreases body weight; prevention of weight regain; safety and tolerability

时间窗: 2 Years

次要结局

  • Decreases waist circumference, decreases the proportion of patients with metabolic syndrome, decreases triglycerides, decreases non-HDL-C, decreases LDL-C, decreases fasting insulin, decreases FPG; increases HDL-C, increases insulin sensitivity(2 Years)

研究者

申办方类型
Industry
责任方
Sponsor

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