ナルコレプシー成人患者におけるTAK-994の研究
基本情報
- NCT ID
- NCT04820842
- ステータス
- 中止
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 26
- 治験依頼者名
- Takeda
概要
Adults with narcolepsy who have completed the TAK-994-1501 study will be able to take part in this study. The main aim of this study is to check if participants have side effects from TAK-994. Participants will take one of 3 different TAK-994 dose for 8 weeks. Then, half the participants will continue with their dose of TAK-994 and half will take a placebo. In this study, a placebo will look like a TAK-994 tablet but will not have any medicine in it. Participants will take TAK-994 or placebo for 4 weeks. Participants will visit the clinic for a final check-up 2 weeks after their last dose of TAK-994 or placebo. The study doctors will check for side effects from TAK-994 and placebo throughout the study. Participants will continue to record any narcolepsy symptoms as they did in Part B of the TAK 994-1501 study.
対象疾患
介入
依頼者(Sponsor)
実施施設 (14)
医療法人社団英和美月会 高田クリニック
Fukuoka, Fukuoka, Japan
Jinyukai Kotorii Isahaya Hospital Dept of Psychiatry
Isahaya-shi, Nagasaki, Japan
Shunkaikai Inoue Hospital Dept of Respiratory Medicine
Nagasaki, Nagasaki, Japan
Kyowakai Hannan Hospital Dept of Psychiatry
Sakai-shi, Osaka, Japan
青山・表参道睡眠ストレスクリニック
Shinagawa-ku, Tokyo-To, Japan
スリープ・サポート クリニック
Shinagawa-ku, Tokyo-To, Japan
Kurume University Hospital Dept of Neuropsychiatry
Kurume-shi, Fukuoka, Japan
医療法人GSGL会 福岡浦添クリニック
Shibuya-ku, Tokyo-To, Japan
Sumida Hospital Phase I
Sumida-ku, Tokyo-To, Japan
大阪回生病院
Osaka, Osaka, Japan
さくらい循環器・内科クリニック
Yokohama, Kanagawa, Japan
Koishikawa Tokyo Hospital Dept of Psychiatry
Bunkyō City, Tokyo-To, Japan
学校法人日本大学 日本大学医学部附属板橋病院
Itabashi-ku, Tokyo-To, Japan
You Ariyoshi Sleep Clinic Dept of Psychiatry
Kitakyushu-shi, Fukuoka, Japan