A Study of Nipocalimab in Adult Participants With Active Systemic Lupus Erythematosus
Part of paid clinical trials in Los Alamitos, California.
- Sponsor
- Janssen Research & Development, LLC
- Study ID
- NCT04882878
- Phase
- PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 65 Years
- Healthy Volunteers
- Not accepted
Interventions
- Placebo — OTHERPlacebo will be administered intravenously.
- Nipocalimab — DRUGNipocalimab dose 1 and dose 2 will be administered intravenously.
- Standard-of-care treatment — DRUGStandard-of-care treatment including immunomodulators, antimalarial drugs and GCs will be administered orally.
Study Details
The purpose of this study is to evaluate the efficacy of nipocalimab versus placebo in participants with active systemic lupus erythematosus (SLE).
Key Dates
- Start date
- Aug 20, 2021
- Status verified
- Dec 2025
- Primary completion
- Apr 30, 2024
- Completion
- Dec 26, 2024
Study Design
- Enrollment
- 228 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Placebo Comparator: Group 1: PlaceboParticipants will receive placebo intravenously (IV) every two weeks (q2w) through Week 50 along with standard-of-care treatments (that is, immunomodulators, antimalarial drugs and Glucocorticoids \[GCs\]).
- Experimental: Group 2: Nipocalimab Dose 1Participants will receive nipocalimab dose 1 intravenously (IV) q2w through Week 50 along with standard-of-care treatments (that is, immunomodulators, antimalarial drugs and GCs).
- Experimental: Group 3: Nipocalimab Dose 2Participants will receive nipocalimab dose 2 intravenously (IV) q2w through Week 50 along with standard-of-care treatments (that is, immunomodulators, antimalarial drugs and GCs).
Primary Outcome Measure
Percentage of Participants Achieving an Systemic Lupus Erythematosus (SLE) Responder Index (SRI)-4 Composite Response at Week 24 [ Time Frame: Week 24 ]
Locations (21)
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