drugset / Trial / NCT00906399

Efficacy and Safety Study of Peginterferon Beta-1a in Participants With Relapsing Multiple Sclerosis

NCT00906399

Phase 3 Completed 1516 enrolled Biogen
RandomizedParallel-groupTriple-blindTreatment

Summary

The primary objective of this study is to determine the efficacy of peginterferon beta-1a in reducing the annualized relapse rate (ARR) in participants with relapsing multiple sclerosis (RMS) at 1 year. The secondary objectives of this study are to determine whether peginterferon beta-1a, at 1 year when compared with placebo, is effective in reducing the total number of new or newly enlarging T2 hyperintense lesions on brain magnetic resonance imaging (MRI) scans, reducing the proportion of participants who relapse, and slowing the progression of disability.

Timeline

Start
2009-06
Primary completion
2012-10
Completion
2013-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject peginterferon beta-1a Protein / enzyme biologic 125 ug Subcutaneous