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临床试验/2025-524217-89-00
2025-524217-89-00招募中4 期

An open label, randomized, single-dose, two-treatment, two-period, cross-over bioequivalence study comparing Pyridostigmine Bromide, P.R.Tab, 180 mg/tab, VIANEX S.A., Greece versus Mestinon® retard 180 mg/prolonged-release tablet, Viatris Healthcare GmbH, Germany, in healthy male and female volunteers under fasting conditions.

Vianex S.A.1 个研究点 分布在 1 个国家目标入组 44 人开始时间: 2025年12月1日最近更新:

试验速览

阶段
4 期
状态
招募中
发起方
入组人数
44
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)
接受健康志愿者

入选标准

  • 未提供

排除标准

  • 未提供

研究者

发起方
Vianex S.A.
申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

George Florakis

Scientific

Vianex S.A.

研究点 (1)

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