41
Participants
Start Date
February 29, 2008
Primary Completion Date
May 31, 2009
Study Completion Date
January 31, 2011
adalimumab
40 mg or 80 mg every other week, subcutaneous
Site Reference # / Investigator 46791, Aichi
Site Reference # / Investigator 46789, Fukui
Site Reference # / Investigator 46798, Fukuoka
Site Reference # / Investigator 46799, Fukuoka
Site Reference # / Investigator 46796, Hiroshima
Site Reference # / Investigator 46782, Hokkaido
Site Reference # / Investigator 7297, Hokkaido
Site Reference # / Investigator 46795, Hyōgo
Site Reference # / Investigator 46797, Kagawa
Site Reference # / Investigator 46787, Kanagawa
Site Reference # / Investigator 46790, Nagano
Site Reference # / Investigator 46793, Osaka
Site Reference # / Investigator 46794, Osaka
Site Reference # / Investigator 46783, Saitama
Site Reference # / Investigator 46784, Saitama
Site Reference # / Investigator 46792, Shiga
Site Reference # / Investigator 46785, Tokyo
Site Reference # / Investigator 46786, Tokyo
Site Reference # / Investigator 46788, Toyama
Lead Sponsor
Eisai Co., Ltd.
INDUSTRY
Abbott
INDUSTRY