drugset / Trial / NCT05376319

PR3-AAV Resilient Remission or PRRR

NCT05376319 ↗

Phase 2 Terminated 6 enrolled Mayo Clinic Genentech, Inc. · collab
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to evaluate the efficacy and safety of obinutuzumab for the treatment of proteinase 3 Anti-Neutrophil Cytoplasmic Antibody (ANCA)-Associated Vasculitis (PR3-AAV).

Timeline

Start
2023-06-30
Primary completion
2024-05-07
Completion
2024-05-07

Outcome

Outcome not reported

Stopped (Business): “Funding was withdrawn by sponsor.”

Drugs

EvaluationDrugModalityDoseRoute
Subject Obinutuzumab Monoclonal antibody 1000 mg Intravenous
Comparator Rituximab Monoclonal antibody 1000 mg Intravenous