180
Participants
Start Date
November 30, 2005
Primary Completion Date
April 30, 2008
Study Completion Date
April 30, 2008
Anti IL-12 monoclonal antibody/ABT-874
Please see Arm Description for intervention description and details.
placebo
12 doses
Site Reference ID/Investigator# 3366, Norfolk
Site Reference ID/Investigator# 3347, Alpharetta
Site Reference ID/Investigator# 994, Nashville
Site Reference ID/Investigator# 992, Cincinnati
Site Reference ID/Investigator# 993, Indianapolis
Site Reference ID/Investigator# 3348, Skokie
Site Reference ID/Investigator# 3349, St Louis
Site Reference ID/Investigator# 796, Houston
Site Reference ID/Investigator# 2081, Salt Lake City
Site Reference ID/Investigator# 3351, San Diego
Site Reference ID/Investigator# 991, Lake Oswego
Site Reference ID/Investigator# 3367, Portland
Site Reference ID/Investigator# 989, Seattle
Site Reference ID/Investigator# 990, Boston
Site Reference ID/Investigator# 3346, Johnston
Site Reference ID/Investigator# 3350, Dallas
Site Reference ID/Investigator# 3361, Halifax
Site Reference ID/Investigator# 985, Laval
Site Reference ID/Investigator# 987, London
Site Reference ID/Investigator# 3364, Montreal
Site Reference ID/Investigator# 794, North Bay
Site Reference ID/Investigator# 988, Québec
Site Reference ID/Investigator# 795, Waterloo
Site Reference ID/Investigator# 3360, Windsor
AbbVie (prior sponsor, Abbott)
INDUSTRY