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)
| 대상 질환 | Psoriatic Arthritis |
|---|---|
| 임상 단계 | 3상 |
| 스폰서 | AbbVie |
| 상태 | 완료 |
| 참여자 수 | 444 명 |
| 중재(약물) | Risankizumab |
| 시작일 | 2019년 3월 7일 |
| 완료일 | 2020년 6월 22일 |
| 결과 공개일 | 2022년 3월 2일 |
요약
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
| Placebo | 26.5 percentage of participants |
|---|---|
| Risankizumab | 51.3 percentage of participants |
| p-value | <0.001 |
|---|---|
| Response Rate Difference | 24.5 (95% CI 15.9–33.0) |
BENITIONS에서 보기 ClinicalTrials.gov 원문 보기
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