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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

Narcolepsy Type 1 (NT 1)

介入

TAK-994(DRUG)
Placebo(DRUG)

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