41
Participants
Start Date
August 31, 2008
Primary Completion Date
April 30, 2010
Study Completion Date
April 30, 2010
catridecacog
35 IU/kg body weight, i.v. administration, once every 4 weeks
Novo Nordisk Investigational Site, Vienna
Novo Nordisk Investigational Site, Graz
Novo Nordisk Investigational Site, Zurich
Novo Nordisk Investigational Site, Marseille
Novo Nordisk Investigational Site, Atlanta
Novo Nordisk Investigational Site, Tampa
Novo Nordisk Investigational Site, Montpellier
Novo Nordisk Investigational Site, Vicenza
Novo Nordisk Investigational Site, Braunschweig
Novo Nordisk Investigational Site, Seville
Novo Nordisk Investigational Site, Columbus
Novo Nordisk Investigational Site, Duisburg
Novo Nordisk Investigational Site, Detroit
Novo Nordisk Investigational Site, East Lansing
Novo Nordisk Investigational Site, Petah Tikva
Novo Nordisk Investigational Site, Tel Litwinsky
Novo Nordisk Investigational Site, Bonn
Novo Nordisk Investigational Site, Minneapolis
Novo Nordisk Investigational Site, Oklahoma City
Novo Nordisk Investigational Site, Orange
Novo Nordisk Investigational Site, Le Kremlin-Bicêtre
Novo Nordisk Investigational Site, Seattle
Novo Nordisk Investigational Site, Phoenix
Novo Nordisk Investigational Site, Boston
Novo Nordisk Investigational Site, Klagenfurt
Novo Nordisk Investigational Site, Toronto
Novo Nordisk Investigational Site, Helsinki
Novo Nordisk Investigational Site, Barcelona
Novo Nordisk Investigational Site, Aberdeen
Novo Nordisk Investigational Site, Birmingham
Novo Nordisk Investigational Site, Bradford
Novo Nordisk Investigational Site, Bristol
Novo Nordisk Investigational Site, Liverpool
Novo Nordisk Investigational Site, London
Novo Nordisk Investigational Site, Newcastle upon Tyne
Lead Sponsor
Novo Nordisk A/S
INDUSTRY