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临床试验/NCT00482196
NCT00482196已完成2 期

To Study Different Levels of MK0493 for Safety, Efficacy, and Tolerability in Obese Patients (0493-017)(COMPLETED)

Merck Sharp & Dohme LLC0 个研究点目标入组 173 人开始时间: 2005年7月1日最近更新:
适应症
相关药物

试验速览

阶段
2 期
状态
已完成
入组人数
173

研究概览

简要总结

To study different doses of MK0493 for safety, efficacy and tolerability in obese patients.

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
21 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patient is between 21 and 65 years of age

排除标准

  • •HIV positive as determined by medical history
  • •Patient is pregnant, lactating or plans to become pregnant
  • •Patient has undergone surgical treatment for obesity
  • •Patient has undergone a surgical procedure within 4 weeks prior to Visit 1 or plans to undergo a surgical procedure during the study
  • •Patient plans to consume more than 2 glasses of grapefruit juice per day during the study
  • •Patient has participated in another clinical study (involving an investigational drug) within 3 months prior to restudy screening

研究者

申办方类型
Industry
责任方
Sponsor

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