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临床试验/2024-512770-10-00
2024-512770-10-00已完成4 期

An open label, balanced, randomized, two-treatment, four period, two-sequence, multiple-dose (steady-state), fully-replicate crossover bioequivalence study comparing Upadacitinib Prolonged Release Tablets 15 mg, manufactured by Sun Pharmaceutical Industries Limited, India with 15 mg prolonged-release tablets (Upadacitinib), Marketing Authorization Holder: AbbVie Deutschland GmbH & Co. KG Knollstraße 67061 Ludwigshafen Germany, in healthy adult, human subjects under fasting condition.

Sun Pharmaceutical Industries Limited1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2024年7月15日最近更新:

试验速览

阶段
4 期
状态
已完成
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)
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

Arshad Khuroo

Scientific

Sun Pharmaceutical Industries Limited

研究点 (1)

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