A Study of the Efficacy and Tolerance of Remicade in the Treatment of Active Ankylosing Spondylitis (Study P04042)(COMPLETED)

PHASE4CompletedINTERVENTIONAL
Enrollment

42

Participants

Timeline

Start Date

October 1, 2004

Primary Completion Date

June 1, 2007

Study Completion Date

June 1, 2007

Conditions
Spondylitis, Ankylosing
Interventions
BIOLOGICAL

Infliximab

Remicade 5 mg/kg, given as an intravenous infusion over a 2-hour period followed by additional 5 mg/kg infusion doses at 2 and 6 weeks after the first infusion, then every 6 to 8 weeks (maximum 9 infusions).

All Listed Sponsors
lead

Merck Sharp & Dohme LLC

INDUSTRY

NCT00779012 - A Study of the Efficacy and Tolerance of Remicade in the Treatment of Active Ankylosing Spondylitis (Study P04042)(COMPLETED) | Biotech Hunter | Biotech Hunter