成人成長ホルモン欠乏症(AGHD)患者に対するソグロヤ®の長期安全性情報追跡調査
基本情報
- NCT ID
- NCT05718570
- ステータス
- 招待制
- 試験のフェーズ
- -
- 試験タイプ
- 観察
- 目標被験者数
- 400
- 治験依頼者名
- Novo Nordisk A/S
概要
In this study, the general long-term safety and effectiveness of Sogroya (somapacitan) in adults with growth hormone deficiency (AGHD) being treated per normal clinical practice is looked into. In the study, information on side effects and how well Sogroya (somapacitan) works during long term treatment in people with Adult Growth Hormone Deficiency (AGHD) will be collected and analysed. Participants will be treated with Sogroya (somapacitan) as prescribed by the study doctor, in accordance with normal clinical practice. The study will last for 5-10 years, depending on when the participant join the study. The participant will be asked to complete two short questionnaires during every visit to the clinic. The questionnaires will collect information on the participant's well-being, work ability and ability to perform daily activities.
対象疾患
介入
依頼者(Sponsor)
実施施設 (6)
Kobe University Hospital_Diabetes and Endocrinology
Kobe-shi, Hyogo, Japan
日本医科大学武蔵小杉病院
Kawasaki-shi, Kanagawa, Japan
地方独立行政法人 大阪府立病院機構 大阪国際がんセンター
Osaka-shi, Osaka, Japan
鹿児島大学病院
Kagoshima-shi, Kagoshima, Japan
福岡大学筑紫病院
Chikushino-shi, Fukuoka, Japan
岡山大学病院
Okayama-shi, Okayama, Japan