A Study to Assess the Safety and Effectiveness of Golimumab in Filipino Patients With Rheumatoid Arthritis, Psoriatic Arthritis and Ankylosing Spondylitis

WithdrawnOBSERVATIONAL
0
Timeline

Start Date

July 31, 2013

Primary Completion Date

July 31, 2016

Study Completion Date

July 31, 2016

Conditions
Rheumatoid ArthritisPsoriatic ArthritisAnkylosing Spondylitis
Interventions
DRUG

No intervention

This is an observational study. Golimumab will be administered as per the recommended doses. Golimumab 50 mg will be given as a subcutaneous injection once a month, on the same date each month. For rheumatoid arthritis: Golimumab 2 mg/kg will be given as a 30 minute intravenous infusion at Weeks 0 and 4, then every 8 weeks thereafter.

Sponsors
All Listed Sponsors
lead

Janssen Pharmaceutica

INDUSTRY