87
Participants
Start Date
October 31, 2004
Primary Completion Date
April 30, 2008
Study Completion Date
April 30, 2008
cetuximab
Initial dose of 400 mg/m2 intravenously (i.v.) over 120 minutes, followed by 250 mg/m2 weekly i.v. over 60 minutes
ImClone Investigational Site, Armonk
ImClone Investigational Site, East Setauket
ImClone Investigational Site, Sellingsgrove
ImClone Investigational Site, Durham
ImClone Investigational Site, Ormond Beach
ImClone Investigational Site, Jacksonville
ImClone Investigational Site, Orlando
ImClone Investigational Site, Louisville
ImClone Investigational Site, Lexington
ImClone Investigational Site, Indianapolis
ImClone Investigational Site, Evansville
ImClone Investigational Site, Kalamazoo
ImClone Investigational Site, Gurnee
ImClone Investigational Site, St Louis
ImClone Investigational Site, Metairie
ImClone Investigational Site, Arlington
ImClone Investigational Site, Temple
ImClone Investigational Site, Bryan
ImClone Investigational Site, Los Angeles
ImClone Investigational Site, Campbell
ImClone Investigational Site, Soquel
ImClone Investigational Site, Boston
ImClone Investigational Site, Ann Arbor
ImClone Investigational Site, Oshawa
ImClone Investigational Site, Ottawa
ImClone Investigational Site, Toronto
ImClone Investigational Site, Toronto
Collaborators (1)
Bristol-Myers Squibb
INDUSTRY
Eli Lilly and Company
INDUSTRY