16
Participants
Start Date
May 31, 2009
Primary Completion Date
September 30, 2010
Study Completion Date
July 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
Innsbruck
New York
New York
Quimper
Atlanta
Bordeaux
Tours
Saint-Priest-en-Jarez
Nantes
Essen
Fort Wayne
Aachen
Lyon
Paris
Grapevine
Houston
Newcastle
Lead Sponsor
Alexion Pharmaceuticals, Inc.
INDUSTRY