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短腸症候群の日本人患者におけるテドグルチドの研究
基本情報
- NCT ID
- NCT05023382
- ステータス
- 募集中
- 試験のフェーズ
- -
- 試験タイプ
- 観察
- 目標被験者数
- 120
- 治験依頼者名
- Takeda
概要
The main aims of this study are to check for side effects from treatment with teduglutide (Revestive) and how well teduglutide controls symptoms of short bowel syndrome. The study sponsor will not be involved in how the participants are treated but will provide instructions on how the clinics will record what happens during the study. During the study, participants with short bowel syndrome will receive an injection of teduglutide just under the skin (subcutaneous) according to their clinic's standard practice. The study doctors will check for side effects from teduglutide for 36 months.
対象疾患
Short Bowel Syndrome
介入
Teduglutide(DRUG)
依頼者(Sponsor)
武田薬品工業株式会社(INDUSTRY)