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临床试验/2023-505335-12-00
2023-505335-12-00撤回4 期

Open label, four-period, two-sequence, fully replicated, randomized, single dose pivotal study for the assessment of bioequivalence between Furosemide 500 mg tablets (Test) and Lasix 500 mg tablets (Reference) in healthy male volunteers under fasting conditions

Ratiopharm GmbH1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2023年10月16日最近更新:

试验速览

阶段
4 期
状态
撤回
入组人数
50
试验地点
1

研究概览

简要总结

暂无简介。

入排标准

年龄范围
18 years 至 64 years(18-64 Years)
性别
Male
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究者

申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Constanze Scheel

Scientific

Ratiopharm GmbH

研究点 (1)

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