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Natalizumab Subcutaneous Immunogenicity and Safety Study — SIMPLIFY  

Relapsing Multiple Sclerosis Clinical Trial

Official title:
A Multicenter, Open-Label Immunogenicity and Safety Study of Subcutaneous Natalizumab 300 mg Administered to Subjects With Relapsing Multiple Sclerosis

Clinical Trial Summary

The primary objective of this study is to evaluate the immunogenicity of natalizumab (BG00002) 300 mg subcutaneous (SC) administered to participants with relapsing multiple sclerosis (RMS). The secondary objectives of the study are to evaluate the safety of natalizumab SC injections and to evaluate the efficacy of natalizumab SC injections on relapses and on new magnetic resonance imaging (MRI) lesions.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02142192
Study type Interventional
Source Biogen
Contact
Status Terminated
Phase Phase 2
Start date December 1, 2014
Completion date June 4, 2015
View Details
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