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リゲリズマブによる以前の臨床試験を完了した慢性特発性蕁麻疹患者におけるリゲ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
- NCT04210843
- 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
- 1,033
- 治験依頼者名
- Novartis
概要
The purpose of this extension study was to establish efficacy and safety of ligelizumab. This was assessed in adult and adolescent chronic spontaneous urticaria (CSU) patients who had completed a preceding ligelizumab study and have relapsed, following treatment in these preceding studies, despite standard of care H1-antihistamine (H1-AH) treatment. This study also fulfilled the Novartis commitment to provide post-trial access to patients who had completed studies: CQGE031C2302 (NCT03580369), CQGE031C2303 (NCT03580356), CQGE031C2202 (NCT03437278) or CQGE031C1301 (NCT03907878).
対象疾患
Chronic Spontaneous Urticaria
介入
Ligelizumab(DRUG)
依頼者(Sponsor)
ノバルティスファーマ株式会社(INDUSTRY)