154
Participants
Start Date
April 30, 2009
Primary Completion Date
March 31, 2010
Study Completion Date
November 30, 2010
adalimumab
Subcutaneous injection using prefilled syringe containing adalimumab 40 mg in 0.8 milliliters
Placebo
Subcutaneous injection using prefilled syringe containing 0.8 milliliters
Site Ref # / Investigator 18683, Copenhagen NV
Site Ref # / Investigator 18684, Roskilde
Site Ref # / Investigator 19141, New York
Site Ref # / Investigator 18208, New York
Site Ref # / Investigator 18981, Hershey
Site Ref # / Investigator 18464, Philadelphia
Site Ref # / Investigator 18206, Norfolk
Site Ref # / Investigator 18469, Kiel
Site Ref # / Investigator 19001, Winston-Salem
Site Ref # / Investigator 18209, Atlanta
Site Ref # / Investigator 18204, Miami
Site Ref # / Investigator 19062, Birmingham
Site Ref # / Investigator 18211, Evansville
Site Ref # / Investigator 18202, Skokie
Site Ref # / Investigator 18461, St Louis
Site Ref # / Investigator 18466, Omaha
Site Ref # / Investigator 18463, San Antonio
Site Ref # / Investigator 18467, Los Angeles
Site Ref # / Investigator 18207, San Diego
Site Ref # / Investigator 18201, Bakerfield
Site Ref # / Investigator 18203, Boston
Site Ref # / Investigator 18210, Boston
Site Ref # / Investigator 19061, Dallas
Site Ref # / Investigator 18471, Dessau
Site Ref # / Investigator 18470, Amsterdam
Site Ref # / Investigator 18468, Rotterdam
Lead Sponsor
Abbott
INDUSTRY