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)
Part of paid clinical trials in Anniston, Alabama.
- Sponsor
- AbbVie
- Study ID
- NCT03671148
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
- Psoriatic Arthritis (PsA)
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Placebo — BIOLOGICALPlacebo for risankizumab administered by subcutaneous (SC) injection
- Risankizumab — BIOLOGICALRisankizumab administered by subcutaneous (SC) injection
Study Details
The purpose of this study is to evaluate the safety and efficacy of risankizumab in adults with moderately to severely active psoriatic arthritis (PsA).
Key Dates
- Start date
- Mar 7, 2019
- Status verified
- Aug 2025
- Primary completion
- Jun 22, 2020
- Completion
- Jun 30, 2026
Study Design
- Enrollment
- 444 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: RisankizumabParticipants randomized to receive 150 mg risankizumab administered by subcutaneous injection at Week 0, Week 4, and Week 16 in Period 1. At Week 24 participants will receive blinded placebo followed by open-label 150 mg risankizumab at Week 28, and every 12 weeks thereafter in Period 2 until the final dosing time point at Week 316.
- Placebo Comparator: PlaceboParticipants randomized to receive double-blind placebo at Week 0, Week 4, and Week 16 in Period 1. At Week 24 participants will receive 150 mg risankizumab followed by open-label 150 mg risankizumab at Week 28, and every 12 weeks thereafter in Period 2 until the final dosing time point at Week 316.
Primary Outcome Measure
Percentage of Participants With an American College of Rheumatology 20% (ACR20) Response at Week 24 [ Time Frame: Baseline and Week 24 ]
Locations (55)
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