drugset / Trial / NCT05441826

Efficacy and Safety of VB119 in Subjects With Minimal Change Disease (MCD) and Focal Segmental Glomerulosclerosis (FSGS)

NCT05441826 ↗

Phase 2 Terminated 1 enrolled Tenet Medicines
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

EvaluationDrugModalityDoseRoute
Subject Budoprutug Monoclonal antibody 100 mg Intravenous
Subject Budoprutug Monoclonal antibody 200 mg Intravenous