JPRN-jRCT2080221803未知3 期
An Open Label Extension Study of Phase III Clinical Trial of Duloxetine in Patients With Fibromyalgia
适应症
试验速览
- 阶段
- 3 期
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- >= 20age old 至 <= 74age old（—）
- 性别
- All
入选标准
- •Participants who have completed the 15-week treatment in the preceding study (A Phase III clinical trial of duloxetine in participants with fibromyalgia), etc.
排除标准
- •Participants with pain caused by diseases other than fibromyalgia and which possibly has any effect to the assessment, etc.
研究者
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This is a study for adults (18-75 years) who have successfully completed treatment either with Dupilumab or with Upadacitinib in the M16-046 study. At the end of M16-046, they have the option to receive Upadacitinib with a duration of 52 weeks beyond the timeframe of Study M16-046. There will be a 30 day follow-up visit after the treatment period is completedModerate to severe Atopic DermatitisMedDRA version: 21.1Level: LLTClassification code 10003639Term: Atopic dermatitisSystem Organ Class: 100000004858EUCTR2019-001227-12-IEAbbVie Deutschland GmbH & Co. KG485
进行中（未招募）
1 期
This is a study for adults (18-75 years) who have successfully completed treatment either with Dupilumab or with Upadacitinib in the M16-046 study. At the end of M16-046, they have the option to receive Upadacitinib with a duration of 52 weeks beyond the timeframe of Study M16-046. There will be a 30 day follow-up visit after the treatment period is completedModerate to severe Atopic DermatitisMedDRA version: 21.1Level: LLTClassification code 10003639Term: Atopic dermatitisSystem Organ Class: 100000004858EUCTR2019-001227-12-HRAbbVie Deutschland GmbH & Co. KG600