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

Outcome

Mixed primary results

registry analysis (superiority or other test); Interferon Beta-1a vs Alemtuzumab; p = 0.2173; Hazard Ratio (HR) 0.70 (95% CI 0.40 to 1.23) NCT00530348 ↗

registry NUMBER Interferon Beta-1a: 11.12 (7.32 to 16.71) percentage of participants with SAD NCT00530348 ↗

registry analysis (superiority or other test); Interferon Beta-1a vs Alemtuzumab; p <0.0001; Rate ratio 0.45 (95% CI 0.32 to 0.63) NCT00530348 ↗

registry NUMBER Interferon Beta-1a: 0.39 (0.29 to 0.53) relapses per participant per year NCT00530348 ↗

registry NUMBER Alemtuzumab: 0.18 (0.13 to 0.23) relapses per participant per year NCT00530348 ↗

Publications

Drugs

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