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临床试验/NCT00340327
NCT00340327已完成1 期

An Ascending Single Dose Study of the Safety and Pharmacokinetics of IMA-638 Administered to Healthy Japanese Subjects

Wyeth is now a wholly owned subsidiary of Pfizer1 个研究点 分布在 1 个国家开始时间: 2006年6月1日最近更新:
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试验速览

阶段
1 期
状态
已完成
发起方
试验地点
1
主要终点
Safety will be measured by evaluating physical examinations, vital signs, electrocardiograms (ECGs), and clinical laboratory test results.

研究概览

简要总结

The purpose of this study is to evaluate the safety and drug levels for single, ascending doses of IMA-638 in healthy Japanese subjects.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Diagnostic
盲法
Double

入排标准

年龄范围
20 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • First generation healthy Japanese men and women of non-childbearing potential.

排除标准

  • 未提供

结局指标

主要结局

Safety will be measured by evaluating physical examinations, vital signs, electrocardiograms (ECGs), and clinical laboratory test results.

次要结局

  • Drug levels and associated biomarkers will be evaluated.

研究者

发起方
Wyeth is now a wholly owned subsidiary of Pfizer
申办方类型
Industry

研究点 (1)

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Study Evaluating IMA-638 in Healthy Japanese | 临床试验