82
Participants
Start Date
March 31, 2007
Primary Completion Date
March 31, 2009
Study Completion Date
November 30, 2010
adalimumab
Subcutaneous injection of 40 mg adalimumab (0.8 mL/injection) every other week (eow)
Placebo
Subcutaneous injection of placebo (0.8 mL/injection) every other week (eow)
Site Ref # / Investigator 46965, Aichi
Site Ref # / Investigator 46977, Aichi
Site Ref # / Investigator 46978, Aichi
Site Ref # / Investigator 46979, Aichi
Site Ref # / Investigator 46922, Chiba
Site Ref # / Investigator 46974, Chiba
Site Ref # / Investigator 46970, Ehime
Site Ref # / Investigator 46971, Fukuoka
Site Ref # / Investigator 46985, Fukuoka
Site Ref # / Investigator 46986, Fukuoka
Site Ref # / Investigator 46987, Fukuoka
Site Ref # / Investigator 46968, Hiroshima
Site Ref # / Investigator 46973, Hokkaido
Site Ref # / Investigator 6881, Hokkaido
Site Ref # / Investigator 46982, Hyōgo
Site Ref # / Investigator 46969, Kagawa
Site Ref # / Investigator 46927, Kanagawa
Site Ref # / Investigator 46984, Kochi
Site Ref # / Investigator 46981, Kyoto
Site Ref # / Investigator 46921, Miyagi
Site Ref # / Investigator 46983, Okayama
Site Ref # / Investigator 46966, Osaka
Site Ref # / Investigator 46967, Osaka
Site Ref # / Investigator 46980, Shiga
Site Ref # / Investigator 46964, Shizuoka
Site Ref # / Investigator 46923, Tokyo
Site Ref # / Investigator 46924, Tokyo
Site Ref # / Investigator 46975, Tokyo
Site Ref # / Investigator 46976, Tokyo
Lead Sponsor
Eisai Co., Ltd.
INDUSTRY
Abbott
INDUSTRY