58
Participants
Start Date
July 31, 2006
Primary Completion Date
October 31, 2009
Study Completion Date
October 31, 2009
aflibercept (ziv-aflibercept, AVE0005, VEGF trap, ZALTRAP®)
4.0 mg/kg aflibercept was administered intravenously (IV) over 1 hour once every 2 weeks in the DB period.
Placebo
Placebo was administered intravenously (IV) over 1 hour once every 2 weeks in the DB period.
aflibercept (ziv-aflibercept, AVE0005, VEGF trap, ZALTRAP®)
4.0 mg/kg aflibercept was administered intravenously (IV) over 1 hour once every 2 weeks in the OL period.
Sanofi-Aventis Administrative Office, Bridgewater
Sanofi-Aventis Administrative Office, Vienna
Sanofi-Aventis Administrative Office, Diegem
Sanofi-Aventis Administrative Office, Laval
Sanofi-Aventis Administrative Office, Budapest
Sanofi-Aventis Administrative Office, Mumbai
Sanofi-Aventis Administrative Office, Netanya
Sanofi-Aventis Administrative Office, Barcelona
Sanofi-Aventis Administrative Office, Guildford Surrey
Lead Sponsor
Regeneron Pharmaceuticals
INDUSTRY
Sanofi
INDUSTRY