Drug Use Investigation for Humira® - All Patient Investigation for Rheumatoid Arthritis

NCT01076959 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 7972

Last updated 2012-08-28

Study results available
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Summary

To clarify the following matters:

* Unknown adverse reactions (especially clinically significant adverse reactions)
* Incidence and conditions of occurrence of adverse reactions in the clinical setting
* Factors that may affect the safety and effectiveness of Humira

Conditions

Sponsors & Collaborators

Principal Investigators

  • Toshiro Maeda · Abbott Japan Co.,Ltd

Eligibility

Min Age
16 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2008-06-30
Primary Completion
2011-06-30
Completion
2011-06-30

Countries

  • Japan

Study Locations

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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 NCT01076959 on ClinicalTrials.gov