546
Participants
Start Date
February 28, 2007
Primary Completion Date
September 30, 2009
Study Completion Date
September 30, 2009
dirucotide
500mg, intravenous, every 6mos until regulatory approval, denial or sponsor termination
Vecmilgravis Hospital, Riga
Copenhagen University Hospital, Copenhagen
West Tallinn Central Hospital, Tallinn
Karolinska Universitetssjukhus, Stockholm
Terveystalo Turku Kuvantaminen, Turku
Heinrich Heine Universitaets, Düsseldorf
St. Michaels Hospital, Toronto
Maaslandziekenhuis, Sittard
Hospital Duran I Reynals, Barcelona
Walton Hospital, Liverpool
Collaborators (1)
BioMS Technology Corp.
INDUSTRY
Eli Lilly and Company
INDUSTRY