drugset / Trial / NCT05889299

Study of the Safety and Efficacy of OMS906 in Patients With Paroxysmal Nocturnal Hemoglobinuria

NCT05889299 ↗

Phase 1 Completed 15 enrolled Omeros Corporation
NaSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to assess the safety, tolerability, pharmacokinetics, pharmacodynamics, and preliminary efficacy in patients with Paroxysmal Nocturnal Hemoglobinuria (PNH).

Timeline

Start
2022-12-09
Primary completion
2025-11-03
Completion
2025-11-03

Drugs

EvaluationDrugModalityDoseRoute
Subject ZALTENIBART Monoclonal antibody 5 mg/kg —
Subject ZALTENIBART Monoclonal antibody 8 mg/kg —