126
Participants
Start Date
June 30, 2005
Primary Completion Date
October 31, 2007
Study Completion Date
December 31, 2007
C1 Esterase Inhibitor
Single application of C1-INH administered intravenously by slow injection or infusion at a recommended rate of 4mL/min.
Placebo
Single application of physiological saline solution equivalent to the volume calculated for subjects in the C1-INH 20 U/kg bw arm.
Study Site, The Bronx
Study Site, Hershey
Study Site, Atlanta
Study Site, Weston
Study Site, Cincinnati
Study Site, Plymouth
Study Site, Rapid City
Study Site, Chicago
Study Site, Omaha
Study Site, Shreveport
Study Site, Tulsa
Study Site, Dallas
Study Site, Idaho Falls
Study Site, Granada Hills
Study Site, Eugene
Study Site, Bellingham
Study Site, Boston
Study Site, Buenos Aires
Study Site, Westmead
Study Site, Plovdiv
Study Site, Sofia
Study Site, Edmonton
Study Site, Ottawa
Study Site, Brno
Study Site, Budapest
Study Site, Tel Litwinsky
Study Site, Skopje
Study Site, Grodzisk Mazowiecki
Study Site, Krakow
Study Site, Târgu Mureş
Study Site 1, Moscow
Study Site 2, Moscow
Study Site 3, Moscow
Study Site, Madrid
Study Site, Gothenburg
Study Site, London
Lead Sponsor
CSL Behring
INDUSTRY