Optimization of Treatment With Adalimumab (Humira)

CompletedOBSERVATIONAL
Enrollment

309

Participants

Timeline

Start Date

August 31, 2006

Primary Completion Date

December 31, 2009

Study Completion Date

February 28, 2010

Conditions
Rheumatoid Arthritis (RA)
Interventions
OTHER

DAS28-IOMS

Investigators randomized to DAS28-IOMS will be expected to adapt their therapeutic approaches in relation to the defined targets, i.e. to optimize adalimumab treatment according to individual patient's responses to treatment in order to achieve a DAS28 score of \< 2.4.

OTHER

0SJ-IOMS

Investigators randomized to 0SJ-IOMS will be expected to adapt their therapeutic approaches in relation to the defined targets, i.e. to optimize adalimumab treatment according to individual patient's responses to treatment in order to achieve a swollen joint count of 0.

OTHER

Routine Care (RC)

Investigators randomized to RC will NOT be expected to adapt their therapeutic approaches to a pre-defined target. They will optimize adalimumab treatment according to individual patient's responses to treatment as per routine care and according to their own judgment.

Trial Locations (1)

N6A 4V2

Lawson Health Research Institute, London

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Abbott

INDUSTRY

lead

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER