非分節性白斑の成人患者におけるザソシチニブの研究
基本情報
- NCT ID
- NCT07108283
- ステータス
- 募集中
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 200
- 治験依頼者名
- Takeda
概要
Vitiligo is a long-term autoimmune condition that causes the skin to lose its color. The body's germ-fighting system (immune system) mistakenly attacks the skin cells (melanocytes) which produce the pigment that gives the skin color (melanin). This leads to the formation of patches of skin with less or no pigment (depigmentation). These patches can occur anywhere on the body. In the nonsegmental form of vitiligo, similar patches occur on both sides of the body (symmetrical patches). The main aim of this study is to learn how safe zasocitinib is, how well it works and how well it is tolerated by adults with nonsegmental vitiligo. The participants will receive the study treatment (either zasocitinib or placebo) for up to 1 year (52 weeks). The placebo looks like the zasocitinib capsule but does not have any medicine in it. Participants who receive placebo at the beginning will change to zasocitinib after about 6 months. During the study, participants will visit their study clinic 11 times.
対象疾患
介入
依頼者(Sponsor)
実施施設 (5)
東京医科大学病院
Tokyo, Japan(NOT_YET_RECRUITING)
東邦大学医療センター佐倉病院
Sakura-shi, Chiba, Japan(RECRUITING)
日本医科大学付属病院
Bunkyo-ku, Tokyo, Japan(NOT_YET_RECRUITING)
酒井眼科医院
Nishi-ku, Osaka, Japan(NOT_YET_RECRUITING)
名古屋市立大学病院
Nagoya, Aichi-ken, Japan(NOT_YET_RECRUITING)