Safety, Efficacy and Tolerability of Ianalumab Versus Placebo, Combination With SoC Therapy, in Participants With Active Lupus Nephritis
Part of paid clinical trials in Birmingham, Alabama.
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT05126277
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 100 Years
- Healthy Volunteers
- Not accepted
Interventions
- ianalumab s.c. q4w — DRUGianalumab s.c. q4w in addition to SoC
- ianalumab s.c. q12w — DRUGianalumab s.c. q12w in addition to SoC
- placebo s.c. — DRUGplacebo s.c. q4w in addition to SoC
Study Details
This trial will evaluate efficacy, safety, and tolerability of subcutaneous (s.c.) ianalumab given every 4 weeks (q4w) or every 12 weeks (q12w) compared to placebo, in combination with SoC, in adult participants with active LN
Key Dates
- Start date
- Jul 14, 2022
- Status verified
- May 2026
- Primary completion
- Jun 22, 2027
- Completion
- Feb 11, 2031
Study Design
- Enrollment
- 452 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Arm 1 - ianalumab s.c. q4wianalumab s.c. q4w in addition to standard of care (SoC)
- Experimental: Arm 2 - ianalumab s.c. q12wianalumab s.c. q12w in addition to SoC
- Placebo Comparator: Arm 3 - placebo s.c. q4wPlacebo s.c. q4w in addition to SoC
Primary Outcome Measure
Frequency and percentage of participants achieving stable Complete Renal Response (CRR) [ Time Frame: Week 72 ]
Locations (27)
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