BENITIONSClinical Trial Intelligence

A Study Comparing Risankizumab to Placebo in Participants With Active Psoriatic Arthritis Including Those Who Have a History of Inadequate Response or Intolerance to Biologic Therapy(Ies)

3期 已完成 NCT03671148

适应症Psoriatic Arthritis
分期3期
申办方AbbVie
状态已完成
受试者人数444 人
干预(药物)Risankizumab
开始日期2019年3月7日
完成日期2020年6月22日
结果公布日2022年3月2日

摘要

The purpose of this study is to evaluate the safety and efficacy of risankizumab in adults with moderately to severely active psoriatic arthritis (PsA).

Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 24

Baseline and Week 24 · percentage of participants

Placebo26.5 percentage of participants
Risankizumab51.3 percentage of participants
p-value<0.001
Response Rate Difference24.5 (95% CI 15.9–33.0)

在 BENITIONS 中查看 查看 ClinicalTrials.gov 原文

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本页整理自 ClinicalTrials.gov 的公开数据,不构成医疗建议,也不构成投资建议。请务必咨询专业医师。