drugset / Trial / NCT03608033

Study of the Safety and Efficacy of OMS721 in Patients With Immunoglobulin A (IgA) Nephropathy

NCT03608033

Phase 3 Terminated 360 enrolled Omeros Corporation
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective of this study is to evaluate the effect of OMS721 on 24-hour urine protein excretion (UPE) in IgA nephropathy (IgAN) patients with high baseline proteinuria (high-risk proteinuria group; 24-hour UPE ≥ 2 g/day) assessed at 36 weeks from baseline.

Timeline

Start
2018-04-05
Primary completion
2024-01-12
Completion
2024-01-12

Drugs

EvaluationDrugModalityDoseRoute
Subject narsoplimab Monoclonal antibody