デュピクセント®を開始した喘息患者の登録
基本情報
- NCT ID
- NCT04287621
- ステータス
- 実施中(募集終了)
- 試験のフェーズ
- -
- 試験タイプ
- 観察
- 目標被験者数
- 718
- 治験依頼者名
- Regeneron Pharmaceuticals
概要
The primary objective of the study is to characterize the patients who initiate treatment for asthma with DUPIXENT® in a real-world setting to understand the attributes of treated patients in real life. This includes characterization of: * Patient demographics (eg, gender, age, and race) * Patient baseline characteristics (eg, prior medications and procedures, medical history, asthma history, weight, height) The secondary objectives of the study are: * To characterize real-world use patterns of DUPIXENT® for asthma * To assess the long-term effectiveness of DUPIXENT® in asthma patients in a real-world setting * To assess effectiveness on comorbid type 2 inflammatory conditions in asthma patients treated with DUPIXENT® * To collect long-term safety data on study participants in the real-world setting
対象疾患
介入
実施施設 (12)
獨協医科大学病院
Mibu, Tochigi, Japan
東京女子医科大学病院
Shinjuku-ku, Tokyo, Japan
学校法人帝京大学 帝京大学医学部附属病院
Itabashi-ku, Tokyo, Japan
Hansaki Clinic
Kiyosu-shi, Aichi-ken, Japan
医療法人 きたかみ腎クリニック きたかみ腎クリニック
Chuo-ku, Tokyo, Japan
Incorporated Medical Corporation, Jinyukai, Jinyu Clinic
Nakano Ku, Tokyo, Japan
順天堂大学医学部附属順天堂医院
Bunkyo-ku, Tokyo, Japan
神戸大学医学部附属病院
Kobe, Hyōgo, Japan
北海道大学病院
Kita-ku, Hokkaido, 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, Japan
The Fraternity Memorial Hospital
Sumida-ku, Tokyo, Japan
昭和医科大学病院
Shinagawa-ku, Tokyo, Japan