drugset / Trial / NCT07611214

PRESERVE: LUPKYNIS in Combination With Belimumab, Obinutuzumab or Anifrolumab in Patients With Lupus Nephritis

NCT07611214

Phase 4 Recruiting 150 enrolled Aurinia Pharmaceuticals Inc.
NaSingle-groupOpen-labelTreatment

Summary

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).

Timeline

Start
2026-04-22
Primary completion
2029-03-02
Completion
2029-03-02

Drugs

EvaluationDrugModalityDoseRoute
Subject Anifrolumab Monoclonal antibody
Subject Belimumab Monoclonal antibody
Subject Obinutuzumab Monoclonal antibody
Subject Voclosporin Other / unclassified
Background Mycophenolate Mofetil Small molecule
Background Prednisone Other / unclassified
Background mycophenolic acid Small molecule

Indications