drugset / Trial / NCT00306592

Natalizumab Re-Initiation of Dosing

NCT00306592

Phase 3 Completed 404 enrolled Biogen Elan Pharmaceuticals · collab
NaSingle-groupOpen-labelTreatment

Summary

The primary objectives of this study are to further evaluate the safety of natalizumab (Tysabri®) monotherapy by evaluating the risk of hypersensitivity and immunogenicity following re-exposure to natalizumab, and to confirm the safety of switching to natalizumab from interferon beta (IFN-β), glatiramer acetate (GA), or other multiple sclerosis (MS) therapies.

Timeline

Start
2006-03
Primary completion
2007-12
Completion
2008-02

Drugs

EvaluationDrugModalityDoseRoute
Subject natalizumab Monoclonal antibody 300 mg Intravenous