Special Investigation (Long-term Investigation) in Patients With Crohn's Disease

NCT01464333 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 511

Last updated 2019-05-20

Study results available
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Summary

This study of Humira will be conducted to obtain information on the safety (especially profile of malignant tumors and serious infections) and effectiveness in patients with Crohn's disease who are receiving Humira for a long period of time.

Conditions

Sponsors & Collaborators

  • AbbVie (prior sponsor, Abbott)

    lead INDUSTRY

Principal Investigators

  • AbbVie Inc. · AbbVie

Eligibility

Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-12-16
Primary Completion
2018-03-31
Completion
2018-03-31

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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 NCT01464333 on ClinicalTrials.gov