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特発性肺線維症の急性増悪の治療におけるART-123の臨床試験
基本情報
- NCT ID
- NCT02739165
- ステータス
- 完了
- 試験のフェーズ
- 第3相
- 試験タイプ
- 介入
- 目標被験者数
- 74
- 治験依頼者名
- Asahi Kasei Pharma Corporation
概要
The purpose of this study is to assess the efficacy and safety of the intravenous drip infusion of ART-123 in patients with acute exacerbation of idiopathic pulmonary fibrosis (IPF) in a multicenter, double-blind, randomized, placebo-controlled, parallel group comparison study, and to confirm its superiority over placebo with survival rate on Day 90 as the primary endpoint.
対象疾患
Idiopathic Pulmonary Fibrosis
介入
ART-123(DRUG)
Placebo(DRUG)
依頼者(Sponsor)
旭化成ファーマ(INDUSTRY)