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临床试验/JPRN-UMIN000009540
JPRN-UMIN000009540已完成未知

Evaluation of method of measuring serum insulin glargine concentration after subcutaneous administration of insulin glargine in healthy male subjects. - Evaluation of method of measuring serum insulin glargine concentration

Medical Co. LTA, Clinical Pharmacology Center0 个研究点目标入组 6 人开始时间: 2012年12月15日最近更新:
适应症

试验速览

阶段
未知
状态
已完成
发起方
入组人数
6

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
20years-old 至 40years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1, Subjects with present illness which requires treatment. 2, Subjects with past medical history which was considered not adequate for this study. 3, Subjects with past history of drug allergy. 4, Subjects who took prescribed medicine and/or OTC drug 1 week prior to admission to the clinic. 5. Subjects who donated and/or withdrawn whole blood more than 400mL within 12 weeks, 200mL within 4 weeks, and/or blood component within 2 weeks prior to admission. 6, Subjects who were participated in a clinical trial and administered new compound study drug within 4 weeks, or any kind of study drug within 3 weeks prior to admission. 7, Subjects with history of alcohol and/or drug abuse. 8, Subjects who was judged not appropriate for this study by study physician.

研究者

发起方
Medical Co. LTA, Clinical Pharmacology Center

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