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TYGRIS - ROW: TYSABRI Global Observational Program in Safety - Rest of World — TYGRIS - ROW  

Multiple Sclerosis Clinical Trial

Official title:
TYGRIS - ROW: TYSABRI® Global Observational Program in Safety - Rest of World

Clinical Trial Summary

The primary objective of this study is to determine the incidence and pattern of serious infections, malignancies, and other serious adverse events (SAEs) in participants with multiple sclerosis (MS) treated with TYSABRI (natalizumab).

Clinical Trial Description

The TYSABRI Global Observational Program in Safety for Rest of World (TYGRIS - ROW)is a safety observational cohort program designed to obtain long-term safety data in multiple sclerosis (MS) participants treated with TYSABRI in a clinical practice setting in countries other than the United States and Canada.

The Prescribing Physician will collect participant information at routine clinic visits (using standard data collection tools) at approximately 6-month intervals for 5 years from the first TYSABRI infusion. ;

Study Design

Observational Model: Cohort, Time Perspective: Prospective

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00483847
Study type Observational
Source Biogen
Contact
Status Completed
Phase N/A
Start date September 2006
Completion date November 2014
View Details
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