drugset / Trial / NCT03712345
Safety and Efficacy Study of IFX-1 in add-on to Standard of Care in GPA and MPA
RandomizedParallel-groupTriple-blindTreatment
Summary
The purpose of this study is to investigate the safety and tolerability of two dose regimens of IFX-1 as add-on to standard of care (SOC) in subjects with GPA and MPA compared with placebo.
Timeline
- Start
- 2018-10-15
- Primary completion
- 2020-09-10
- Completion
- 2021-05-03
Outcome
Outcome not reported
Stopped (Enrollment): “Due to COVID-19 pandemic outbreak and its impact on overall study activities. All efforts were made to ensure that participants that were enrolled and/or were still in the study will continue to receive treatment and follow-up until study completion.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | vilobelimab | Monoclonal antibody | — | Intravenous |