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)
Phase 3
Completed
NCT03671148
| Condition | Psoriatic Arthritis |
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| Phase | Phase 3 |
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| Sponsor | AbbVie |
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| Status | Completed |
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| Enrollment | 444 participants |
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| Interventions | Risankizumab |
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| Start date | Mar 7, 2019 |
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| Completion date | Jun 22, 2020 |
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| Results posted | Mar 2, 2022 |
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Summary
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) |
Open in BENITIONS
View on ClinicalTrials.gov
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