Risankizumab Versus Secukinumab for Participants With Moderate to Severe Plaque Psoriasis
Part of paid clinical trials in Glendale, Arizona.
- Sponsor
- AbbVie
- Study ID
- NCT03478787
- Phase
- PHASE3
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- All
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- risankizumab — DRUGSubcutaneous (SC) injection
- secukinumab — DRUGSubcutaneous (SC) injection
Study Details
The main objective of this study is to evaluate the efficacy and safety of risankizumab compared with secukinumab for the treatment of adult subjects with moderate to severe plaque psoriasis who are candidates for systemic therapy.
Key Dates
- Start date
- May 8, 2018
- Status verified
- Jun 2021
- Primary completion
- Jul 8, 2020
- Completion
- Jul 8, 2020
Study Design
- Enrollment
- 327 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: RisankizumabParticipants randomized to risankizumab receive 2 injections of active risankizumab (150 mg total dosage) subcutaneously (SC) at Weeks 0 and 4, and then every 12 weeks (q12w) thereafter until the last dose at Week 40 (Week 64 for participants in France).
- Active Comparator: SecukinumabParticipants randomized to secukinumab receive 2 injections of active secukinumab (300 mg total dosage) SC at Weeks 0, 1, 2, 3, and 4, and then every 4 weeks (q4w) thereafter until the last dose at Week 48.
Primary Outcome Measure
Percentage of Participants With a 90% Reduction From Baseline Psoriasis Area and Severity Index (PASI 90) at Week 16 [ Time Frame: Week 16 ]
Locations (28)
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