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FTY720 in Patients With Primary Progressive Multiple Sclerosis — INFORMS  

Primary Progressive Multiple Sclerosis Clinical Trial

Official title:
A Double-blind, Randomized, Multicenter, Placebo-controlled, Parallel-group Study Comparing the Efficacy and Safety of 0.5mg FTY720 Administered Orally Once Daily Versus Placebo in Patients With Primary Progressive Multiple Sclerosis

Clinical Trial Summary

The purpose of this study is to evaluate whether FTY720 is effective in delaying MS disability progression compared to placebo in patients with PPMS.

Clinical Trial Description

n/a

Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT00731692
Study type Interventional
Source Novartis
Contact
Status Completed
Phase Phase 3
Start date July 2008
Completion date December 2014
View Details
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