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临床试验/2025-521732-11-00
2025-521732-11-00
尚未招募
1 期

Single dose, open-label, laboratory blinded, randomized, 2-treatment, 2-period, 2-sequence, crossover, pivotal study to assess the relative bioavailability of Test Product Naproxen sodium 660 mg modified release tablets to Reference Product Actromadol 660 mg Modified-Release tablets in healthy adult male and female subjects under fed conditions.

Laboratorios Cinfa S.A.1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2026年2月12日最近更新:

概览

阶段
1 期
状态
尚未招募
发起方
Laboratorios Cinfa S.A.
入组人数
32
试验地点
1

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
Laboratorios Cinfa S.A.
申办方类型
Pharmaceutical company
责任方
Principal Investigator
主要研究者

Rubén Rubén Estepa Sanz

Scientific

Laboratorios Cinfa S.A.

研究点 (1)

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