drugset / Trial / NCT00838513

Open Label Controlled Trial of Eculizumab in Adult Patients With Plasma Therapy-sensitive Atypical Hemolytic Uremic Syndrome (aHUS)

NCT00838513

Phase 2 Completed 15 enrolled Alexion Pharmaceuticals, Inc.
Non-randomizedSingle-groupOpen-labelTreatment

Summary

The purpose of this study is to determine whether eculizumab is safe and effective in the treatment of adult patients with plasma therapy-sensitive Atypical Hemolytic-Uremic Syndrome (aHUS).

Timeline

Start
2009-07
Primary completion
2010-10
Completion
2013-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Eculizumab Monoclonal antibody 1200 mg Intravenous