日本人原発性免疫不全症患者を対象としたTAK-664の延長試験
基本情報
- NCT ID
- NCT04842643
- ステータス
- 完了
- 試験のフェーズ
- 第3相
- 試験タイプ
- 介入
- 目標被験者数
- 12
- 治験依頼者名
- Takeda
概要
This study is an extension study for participants with primary immunodeficiency disorders who were previously treated with IGSC, 20% in the TAK-664-3001 study. They must have completed that study or be about to complete it before joining this study. Participants will continue treatment with IGCS, 20% in this study. The main aim of this study is to check for side effects from long-term treatment with IGSC, 20% . This medicine is not yet licensed in Japan, so participants will be treated with IGSC, 20% until it becomes commercially available.
対象疾患
介入
依頼者(Sponsor)
実施施設 (8)
名古屋大学医学部附属病院
Nagoya, Aichi-ken, Japan
久留米大学病院
Kurume, Fukuoka, Japan
National defense medical college Hospital
Tokorozawa, Saitama, Japan
九州大学病院
Fukuoka, Japan
東京歯科大学水道橋病院
Tokyo, Japan
広島大学病院
Hiroshima, Japan
国立大学法人金沢大学附属病院
Kanazawa, Ishikawa-ken, Japan
岐阜大学医学部附属病院
Gifu, Japan