Post Marketing Surveillance of Remicade
NCT00724529 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 938
Last updated 2013-01-23
Summary
The purpose of this study is to understand the safety and effectiveness of infliximab when used in clinical practice. This is a post-marketing surveillance study.
Conditions
Interventions
- BIOLOGICAL
-
Infliximab 5 mg/kg IV given in a schedule according to the official label, based on the indication it is being used for.
Sponsors & Collaborators
-
Janssen Korea, Ltd., Korea
lead INDUSTRY
Principal Investigators
-
Janssen Korea, Ltd., Korea Clinical Trial · Janssen Korea, Ltd., Korea
Eligibility
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2007-06-30
- Primary Completion
- 2011-08-31
- Completion
- 2011-08-31
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