drugset / Trial / NCT04983888

Obinutuzumab in Primary FSGS

NCT04983888 ↗

Phase 2 Completed 20 enrolled Mayo Clinic Genentech, Inc. · collab
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety and efficacy of Obinutuzumab in inducing complete or partial remission of proteinuria.

Timeline

Start
2021-11-17
Primary completion
2025-06-16
Completion
2025-06-16

Drugs

EvaluationDrugModalityDoseRoute
Subject Obinutuzumab Monoclonal antibody 1 g Intravenous