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Clinical Trials/NCT00032799
NCT00032799
Completed
Phase 3

A Phase 3 International, Multicenter, Double-blind, Placebo-controlled Study of the Safety, Efficacy, and Tolerability of Intravenous Antegren (Natalizumab) in Subjects With Moderate to Severely Active Crohn's Disease

Biogen1 site in 1 country905 target enrollmentDecember 2001

Overview

Phase
Phase 3
Intervention
Not specified
Conditions
Crohn's Disease
Sponsor
Biogen
Enrollment
905
Locations
1
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

The purpose of this study is to determine the safety and efficacy of natalizumab in individuals diagnosed with moderately to severely active Crohn's disease. It is thought that natalizumab may stop the movement of certain cells, known as white blood cells, into bowel tissue. These cells are thought to cause damage in the bowel leading to the symptoms of Crohn's disease.

Registry
clinicaltrials.gov
Start Date
December 2001
End Date
September 2003
Last Updated
9 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Biogen
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

Study Sites (1)

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