跳至主要内容
临床试验/JPRN-UMIN000018174
JPRN-UMIN000018174已完成1 期

Clinical pharmacological study of TM5509 -Clinical pharmacological study in male mild obesity subjects- - Clinical pharmacological study of TM5509 -Clinical pharmacological study in male mild obesity subjects- (TM5509-6)

Tohoku university school of medicine, molecular medicine and therapy, Toshio Miyata0 个研究点目标入组 10 人开始时间: 2015年8月10日最近更新:

试验速览

阶段
1 期
状态
已完成
发起方
入组人数
10

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 45years-old(—)
性别
Male

入选标准

  • 未提供

排除标准

  • 1.History of liver diseases, cardiovascular diseases, respiratory diseaases, gastroenteric diseases, kidney diseases, cerebralvascular diseases, cancer 2.Known hypersensitivity to some drugs and foods 3.More than grade 1 in liver function disorders 4.Treatment by other doctors (included supplement) within 14 days before screening 5.Treatment with any investigational compound within 120 days before screening 6.History of TM5509 administration 7.History of blood taken *>= 1200ml of all blood within 1 year before screening *>= 400ml of all blood with 84 days before screening *>= 200ml of all blood within 14 days before screening 8.Smoking status and treatment with anti-nicotine agents 9.Known active chronic hepatitis B or C, active syphilis and human immunodeficiency virus infection 10.Abuse of alcohol or drugs (included past history) 11.Bleeding, in the tendency to bleeding, and family history and past history of bleeding disorders 12.Somebody who are directed by principle investigator and employees in Hamamatsu University hospital 13.Any serious medical or psychiatric illness that could, in the opinion of the investigator, potentially interfere with the completion of treatment according to this protocol.

研究者

发起方
Tohoku university school of medicine, molecular medicine and therapy, Toshio Miyata

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