203
Participants
Start Date
September 30, 2007
Primary Completion Date
September 30, 2008
Humira (adalimumab)
Study drug will be provided as a sterile, preservative-free solution for subcutaneous injection, contained in a pre-filled syringe housed in a pen device (pre-filled pen). Loading dose of 80 mg of adalimumab subcutaneously (sc) at Baseline, and 40 mg of adalimumab sc at Week 1, followed by 40 mg of adalimumab sc every other week (eow) for 24 weeks.
Calgary
Calgary
Edmonton
Surrey
Vancouver
Winnipeg
Winnipeg
Moncton
St. John's
St. John's
Halifax
Barrie
Fenwick
Hamilton
London
London
Markham
Nepean
North Bay
Oakville
Oakville
Toronto
Waterloo
Montreal
Québec
Sherbrooke
Ste-Foy
Lead Sponsor
Abbott
INDUSTRY