drugset / Trial / NCT00202995

Randomized Study Designed to Look at Disease Progression Using 2 Currently FDA Approved Drugs for the Treatment of RRMS

NCT00202995

Phase 4 Terminated 91 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedParallel-groupOpen-labelPrevention

Summary

Randomized study designed to look at the difference in relapse rates between patients remaining on their current interferon medication and those switched to Copaxone®

Timeline

Start
2004-07
Primary completion
2007-10
Completion
2007-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Glatiramer Acetate Small molecule 20 mg Subcutaneous
Comparator Interferon beta-1a Protein / enzyme biologic 44 ug
Comparator Interferon beta-1b Protein / enzyme biologic 250 mg