drugset / Trial / NCT05441826
Efficacy and Safety of VB119 in Subjects With Minimal Change Disease (MCD) and Focal Segmental Glomerulosclerosis (FSGS)
NaSingle-groupOpen-labelTreatment
Summary
Phase 2, multi-center, proof-of-concept study to evaluate the safety and efficacy of VB119 on the maintenance of remission and duration of response in adults with primary MCD or primary FSGS who previously responded to steroid therapy.
Timeline
- Start
- 2022-05-03
- Primary completion
- 2023-05-03
- Completion
- 2023-10-12
Outcome
Outcome not reported
Stopped: “Sponsor change”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Budoprutug | Monoclonal antibody | 100 mg | Intravenous |
| Subject | Budoprutug | Monoclonal antibody | 200 mg | Intravenous |