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临床试验/JPRN-jRCT2080225073
JPRN-jRCT2080225073已完成1 期

Pharmacokinetics in patients with hepatic dysfunction

Kyorin Pharmaceutical Co.,Ltd.0 个研究点目标入组 13 人开始时间: 2020年2月14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
13

研究概览

简要总结

The pharmacokinetic parameters of KRP-AM1977X 75 mg were determined after single oral administration to patients with mild to moderate severity of hepatic dysfunction. The plasma drug concentration of AM-1977 in the moderate patients did not vary significantly compared with the mild patients. No major safety issues were identified in this study.

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 <= 80age old(—)
性别
All

入选标准

  • Person with BMI that is more than 18.5 but less than 30.0, etc.

排除标准

  • Have a history of allergy or severe side effects to quinolone antibiotics.

研究者

发起方
Kyorin Pharmaceutical Co.,Ltd.

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