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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)