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take mycophenolic acid analog (MPAA), either by continuing current MPAA therapy or by initiating it on or before Day 1\n* Willing to take corticosteroids, either by continuing current corticosteroids (prednisone \\[or equivalent\\]) or by initiating on or before Day 1\n\nKey Exclusion Criteria:\n\n* Any B cell targeted therapy except for the concomitant biologics (belimumab and obinutuzumab) within 1 year prior to Screening unless demonstration of B cell count within the normal range\n* Cyclophosphamide or any calcineurin inhibitor other than voclosporin (eg, cyclosporine and tacrolimus) within 3 months prior to Screening\n* Any other immunosuppressive therapy except for the concomitant drugs (anifrolumab, MPAAs and oral prednisone \\[or equivalent\\]) and immunosuppressive agents used to treat a patient's underlying systemic lupus erythematosus (SLE), including, but not limited to, the examples below, within 30 days or 5 half-lives, whichever is longer, prior to Screening:\n\n  * Anti-tumor necrosis factor (TNF) therapy (eg, adalimumab, etanercept, infliximab)\n  * Anti-interleukin therapy (eg, risankizumab, secukinumab, ixekizumab, ustekinumab, guselkumab, tocilizumab, dupilumab)\n  * T cell costimulation modulator (eg, abatacept)\n  * Intravenous immunoglobulin (IVIg)\n  * Janus kinase (JAK) inhibitors (eg, upadacitinib)\n* Pregnant, breastfeeding or intending to become pregnant during the Study","ALL","18 Years","75 Years",{"count":230,"type":231},150,"ESTIMATED","INTERVENTIONAL",[234],"PHASE4","The goal of this clinical study is to assess the efficacy and safety of LUPKYNIS® in combination with belimumab, obinutuzumab or anifrolumab at inducing rapid renal response in patients with lupus nephritis (LN).",[237],"Lupus Nephritis",[21,239],"calcineurin inhibitor","2026-06-11",{"date":242,"type":243},"2026-06-12","ACTUAL",{"date":245,"type":243},"2026-04-22",{"date":247,"type":231},"2029-03-02",{"name":5,"class":6},15]