drugset / Trial / NCT02598583

Dose-Escalation Study of ALXN1210 IV in Participants With Paroxysmal Nocturnal Hemoglobinuria (PNH)

NCT02598583

Phase 1/2 Completed 13 enrolled Alexion Pharmaceuticals, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

This study evaluated the safety, tolerability, efficacy, pharmacokinetics, pharmacodynamics, and immunogenicity of multiple intravenous (IV) doses of ALXN1210 administered to participants with PNH who have not previously been treated with complement inhibitor.

Timeline

Start
2015-11-12
Primary completion
2016-07-14
Completion
2021-03-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Ravulizumab Monoclonal antibody 900 mg Intravenous
Subject Ravulizumab Monoclonal antibody 1800 mg Intravenous