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临床试验/NCT00259896
NCT00259896已完成1 期

A Randomized, Open-label, Placebo-controlled, Repeat-dose Study to Assess the Pharmacokinetics and Pharmacodynamics of 5 Micrograms Exenatide Administered Subcutaneously Twice Daily for 7 Days in Healthy Normal Volunteers and in Subjects With Type 2 Diabetes Mellitus

GlaxoSmithKline0 个研究点目标入组 30 人开始时间: 2005年10月1日最近更新:
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试验速览

阶段
1 期
状态
已完成
入组人数
30
主要终点
Pharmacodynamic measurements during 7 days of dosing.

研究概览

简要总结

This study is a placebo-controlled study in both healthy normal subjects and patients with Type 2 Diabetes Mellitus to assess the levels of exenatide in the bloodstream when it is given for 7 days, and to assess the impact this medication has on various substances in the blood. Assessments include repeat blood sampling and monitoring of any side effects.

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
None

入排标准

年龄范围
18 Years 至 66 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • have type 2 diabetes mellitus that has been diagnosed for at least three months
  • must be taking either (1) no medication for their diabetes or (2) taking metformin, a sulfonylurea, or metformin and a sulfonylurea
  • must be willing to wash-out of these medications for 14 days prior to the start of the study
  • must have bloodwork that meets certain criteria (for example, total cholesterol < 240 mg/dL)

排除标准

  • must not have any other major illness other than diabetes

结局指标

主要结局

Pharmacodynamic measurements during 7 days of dosing.

次要结局

  • Pharmacokinetic measurements during 7 days of dosing.

研究者

申办方类型
Industry
责任方
Sponsor

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