drugset / Trial / NCT05126277

Safety, Efficacy and Tolerability of Ianalumab Versus Placebo, Combination With SoC Therapy, in Participants With Active Lupus Nephritis

NCT05126277

Phase 3 Active not recruiting 452 enrolled Novartis Pharmaceuticals
RandomizedParallel-groupQuadruple-blindTreatment

Summary

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

Timeline

Start
2022-07-14
Primary completion
2027-06-22
Completion
2031-02-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Ianalumab Monoclonal antibody Subcutaneous

Indications