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中等度から重度のアトピー性皮膚炎を有する成人患者に投与されたREGN3500の有効性、安全性、および薬物動態プロファイル
基本情報
- NCT ID
- NCT03738423
- ステータス
- 中止
- 試験のフェーズ
- 第2相
- 試験タイプ
- 介入
- 目標被験者数
- 129
- 治験依頼者名
- Regeneron Pharmaceuticals
概要
The primary objective of the study is to assess the efficacy of REGN3500 monotherapy in Atopic dermatitis (AD), as well as understand the dose-response relationship, compared with placebo treatment, in adult patients with moderate-to-severe AD. Secondary objectives are to: * Assess the safety and tolerability of subcutaneous (SC) doses of REGN3500 monotherapy in adult patients with moderate-to-severe AD * Assess the Pharmacokinetics (PK) of REGN3500 in adult patients with moderate-to-severe AD * Assess the immunogenicity of REGN3500 in adult patients with moderate-to-severe AD
対象疾患
Atopic Dermatitis
介入
REGN3500(DRUG)
REGN3500-Matching Placebo(DRUG)