5
Participants
Start Date
July 31, 2009
Primary Completion Date
October 31, 2010
Study Completion Date
December 31, 2013
eculizumab
All patients received open-label eculizumab administered intravenously on the following dose schedule: Induction dose - 900 mg per week for four weeks and a dose of 1200 mg one week later; Maintenance dose - 1200 mg every two weeks. Patients who received plasma exchange or infusion during the eculizumab treatment period received a supplemental dose of 600 mg within one hour before plasma infusion or within one hour after the completion of each plasma exchange.
Stockholm
Genova
Hanover
Bordeaux
Nantes
Starsbourg
Lyon
Paris
Bois-Guillaume
Toronto
Nijmegen
Exeter
Glasgow
Lead Sponsor
Alexion Pharmaceuticals, Inc.
INDUSTRY