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COVID-19重症肺炎患者における静脈内投与ラブリズマブの有効性および安全性に関する研究
基本情報
- NCT ID
- NCT04369469
- ステータス
- 中止
- 試験のフェーズ
- 第3相
- 試験タイプ
- 介入
- 目標被験者数
- 202
- 治験依頼者名
- Alexion Pharmaceuticals, Inc.
概要
This study evaluated the efficacy, safety, pharmacokinetics, and pharmacodynamics of ravulizumab administered in adult participants with coronavirus disease 2019 (COVID-19) severe pneumonia, acute lung injury, or acute respiratory distress syndrome. Participants were randomly assigned to receive ravulizumab in addition to best supportive care (BSC) (2/3 of the participants) or BSC alone (1/3 of the participants). BSC consisted of medical treatment and/or medical interventions per routine hospital practice.
対象疾患
COVID-19 Severe PneumoniaAcute Lung InjuryAcute Respiratory Distress SyndromePneumonia, Viral
介入
Ravulizumab(BIOLOGICAL)
BSC(OTHER)
依頼者(Sponsor)
アレクシオンファーマ合同会社(INDUSTRY)
実施施設 (3)
東京科学大学病院
Bunkyō City, Tokyo-To, Japan
東京医科大学病院
Shinjuku-Ku, Tokyo, Japan
東京慈恵会医科大学附属病院
Minato-Ku, Tokyo, Japan