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临床试验/NCT00131430
NCT00131430已完成2 期

An 18-Month Study to Assess the Safety, Tolerability, and Efficacy of MK0364 in Obese Patients

Merck Sharp & Dohme LLC0 个研究点目标入组 500 人开始时间: 2005年8月最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
500
主要终点
After 24 weeks, body weight, safety, and tolerability

研究概览

简要总结

A study to determine the safety and efficacy of an investigational drug in patients with obesity.

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

  • Obese patients with a body mass index between 30kg/m2 and 43 kg/m2, inclusive (BMI between 27 kg/m2 and 43kg/m2, inclusive for those with obesity-related comorbidities including hypertension, dyslipidemia and sleep apnea).

排除标准

  • Patients with serious or unstable current or past medical conditions.

结局指标

主要结局

After 24 weeks, body weight, safety, and tolerability

时间窗: After 24 weeks

次要结局

  • After 80 weeks, body weight(After 80 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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