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Clinical Trial Summary

This investigation was conducted to obtain the following information regarding the use of Adalimumab (Humira®) 40mg Syringe 0.8mL for Subcutaneous Injection in patients with Intestinal Behcet's Disease.

1. Incidence and conditions of occurrence of adverse reactions in clinical practice

2. Factors likely to affect the safety and effectiveness


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT01960790
Study type Observational
Source AbbVie
Contact
Status Completed
Phase
Start date May 25, 2013
Completion date May 15, 2017

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