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临床试验/ACTRN12610000287033
ACTRN12610000287033招募中1 期

A phase I randomized, double-blind, placebo-controlled study inhealthy male volunteers to examine the safety, tolerability, and pharmacokinetics of HMPL-011 after multiple dosing for 14days.

Hutchison MediPharma0 个研究点目标入组 24 人开始时间: 2010年4月9日最近更新:
适应症

试验速览

阶段
1 期
状态
招募中
发起方
入组人数
24

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional
分配方式
Randomised controlled trial
主要目的
Treatment

入排标准

年龄范围
18 Years 至 45 Years(—)
性别
Male

入选标准

  • Healthy male subjects having Body Mass Index (BMI) between 19 and 34 kg/m2

排除标准

  • Any significant acute or chronic medical condition. Volunteers at risk of tuberculosis(TB). Evidence of organ dysfunction or any clinically significant deviation from normal.

研究者

发起方
Hutchison MediPharma

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