drugset / Trial / NCT00530348

Comparison of Alemtuzumab and Rebif® Efficacy in Multiple Sclerosis, Study One

NCT00530348

Phase 3 Completed 581 enrolled Genzyme, a Sanofi Company Bayer · collab
RandomizedParallel-groupSingle-blindTreatment

Summary

The purpose of this study was to establish the efficacy and safety of alemtuzumab (Lemtrada™) as a treatment for relapsing-remitting multiple sclerosis (MS), in comparison with subcutaneous (SC) interferon beta-1a (Rebif®). The study had enrolled participants who had not previously received MS disease-modifying therapies. Participants had monthly laboratory tests and comprehensive testing every 3 months.

Timeline

Start
2007-08
Primary completion
2011-04
Completion
2011-04

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Alemtuzumab Monoclonal antibody 12 mg Intravenous
Comparator Interferon beta-1a Protein / enzyme biologic 44 ug Subcutaneous