drugset / Trial / NCT07096843
A Phase 2 Study of Budoprutug in Subjects With Primary Membranous Nephropathy
Non-randomizedSequentialOpen-labelTreatment
Summary
To evaluate the safety and tolerability of three dose regimens of budoprutug in subjects with PMN
Timeline
- Start
- 2025-08-25
- Primary completion
- 2027-10
- Completion
- 2027-10
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Budoprutug | Monoclonal antibody | — | Intravenous |