drugset / Trial / NCT00099502

BEYOND: Betaferon/Betaseron Efficacy Yielding Outcomes of a New Dose in Multiple Sclerosis (MS) Patients

NCT00099502

Phase 3 Completed 2244 enrolled Bayer
RandomizedParallel-groupTriple-blindTreatment

Summary

The purpose of this study is to determine * whether treatment with Betaferon / Betaseron (interferon beta-1b) 500 micrograms safe, tolerable and more efficacious than treatment with interferon beta-1b 250 micrograms * whether treatment with Betaferon / Betaseron (interferon beta-1b) tolerable and more efficacious than treatment with Copaxone (Glatiramer Acetate) 20 mg

Timeline

Start
2003-11
Primary completion
Completion
2007-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Glatiramer Acetate Small molecule 20 mg Subcutaneous
Subject Interferon beta-1b Protein / enzyme biologic 250 ug Subcutaneous
Subject Interferon beta-1b Protein / enzyme biologic 500 ug Subcutaneous