214
Participants
Start Date
December 31, 2003
Primary Completion Date
June 30, 2006
Study Completion Date
November 30, 2011
Abatacept
IV infusions, IV, 10mg/kg body weight, every 4 weeks, 6 months (unless a disease flare discontinued the patient earlier).
Placebo
IV infusions, IV, N/A, every 4 weeks, 6 months.
Abatacept
Solution, intravenous, Approximately 10 mg/kg fixed dose, based on subject's body weight; 500 mg for subjects weighing \< 60kg; 750 mg for subjects weighing 60 to 100 kg; and 1 gram for subjects weighing \> 100 kg, monthly
Omaha
Livingston
New Hyde Park
Valhalla
Cincinnati
Cleveland
Duncansville
Dallas
Seattle
Milwaukee
Local Institution, Bregenz
Local Institution, Botucatu
Local Institution, Rio de Janeiro
Local Institution, São Paulo
Local Institution, Paris
Local Institution, Strasbourg
Local Institution, Berlin
Local Institution, Bremen
Local Institution, Halle
Local Institution, Hamburg
Local Institution, Florence
Local Institution, Genova
Local Institution, Milan
Local Institution, Napoli
Local Institution, Roma
Local Institution, Trieste
Local Institution, Guadalajara
Local Institution, Mexico City
Local Institution, Monterrey
Local Institution, Puebla City
Local Institution, San Luis Potosí City
Local Institution, Lima
Local Institution, Lisbon
Local Institution, A Coruña
Local Institution, Valencia
Local Institution, Lausanne
Lead Sponsor
Bristol-Myers Squibb
INDUSTRY