Post Marketing Surveillance of Remicade

NCT00724529 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 938

Last updated 2013-01-23

No results posted yet for this study

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

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

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00724529 on ClinicalTrials.gov