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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

Primary Immunodeficiency Disease

介入

IGSC 20% infusion(BIOLOGICAL)

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