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 |
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| 分期 | 3期 |
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| 申办方 | AbbVie |
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| 状态 | 已完成 |
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| 受试者人数 | 444 人 |
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| 干预(药物) | Risankizumab |
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| 开始日期 | 2019年3月7日 |
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| 完成日期 | 2020年6月22日 |
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| 结果公布日 | 2022年3月2日 |
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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
| Placebo | 26.5 percentage of participants |
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| Risankizumab | 51.3 percentage of participants |
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| p-value | <0.001 |
| Response Rate Difference | 24.5 (95% CI 15.9–33.0) |
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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。