drugset / Trial / NCT06614985

The Efficacy and Safety of Treatment With Telitacicept in Primary Membranous Nephropathy

NCT06614985

Phase 2 Not yet recruiting 172 enrolled Renmin Hospital of Wuhan University
RandomizedSequentialOpen-labelTreatment

Summary

This is a multiple-center, prospective, open-label, positive drug controlled, randomized, clinical study to evaluate the safety and efficacy of Telitacicept in the treatment of primary membranous nephropathy.

Timeline

Start
2024-10-20
Primary completion
2026-10-01
Completion
2027-10-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclophosphamide Other / unclassified 0.4 g Intravenous
Subject Telitacicept Protein / enzyme biologic 160 mg Subcutaneous
Background Prednisone Other / unclassified Oral