A Study of Ustekinumab in Participants With Active Systemic Lupus Erythematosus
Part of paid clinical trials in Anniston, Alabama.
- Sponsor
- Janssen Research & Development, LLC
- Study ID
- NCT03517722
- Phase
- PHASE3
- Status
- Terminated
Conditions
- Lupus Erythematosus, Systemic
Eligibility Criteria
- Sex
- ALL
- Age
- 16 Years - 75 Years
- Healthy Volunteers
- Not accepted
Interventions
- Placebo — DRUGParticipants will receive placebo matching to ustekinumab IV or SC.
- Ustekinumab (approximately 6 mg/kg) — DRUGParticipants will receive ustekinumab approximately 6 mg/kg via IV route based on body weight-range.
- Ustekinumab 90 mg — DRUGParticipants will receive 90 mg ustekinumab via SC route.
Study Details
The purpose of this study is to evaluate the efficacy of ustekinumab in participants with active systemic lupus erythematosus (SLE) who have not adequately responded to one or more standard of care treatments.
Key Dates
- Start date
- Apr 16, 2018
- Status verified
- Apr 2025
- Primary completion
- Nov 5, 2020
- Completion
- Nov 5, 2020
Study Design
- Enrollment
- 516 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: UstekinumabParticipants will receive ustekinumab approximately 6 milligram per kilogram (mg/kg) intravenously (IV) based on body weight-range at Week 0 followed by 90 mg ustekinumab subcutaneously (SC) at Week 8 and every 8 weeks (q8w) thereafter through Week 48 during double-blind period. Eligible participants who will enter the extension period will continue to receive 90 mg ustekinumab SC q8w through Week 160.
- Experimental: PlaceboParticipants will receive matching placebo to ustekinumab IV at Week 0, followed by matching placebo to ustekinumab SC at Week 8 and q8w thereafter through Week 48 during double-blind period. Eligible participants who will enter the extension period will cross-over to receive 90 mg ustekinumab SC q8w through Week 160.
Primary Outcome Measure
Percentage of Participants Achieving a Systemic Lupus Erythematosus Responder Index-4 (SRI-4) Composite Response at Week 52 [ Time Frame: Week 52 ]
Locations (69)
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