drugset / Trial / NCT00203021

Glatiramer Acetate (Copaxone®) Study to Follow Participants From the First Original Study for Safety and Effectiveness

NCT00203021

Phase 4 Completed 208 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This open-label extension study will evaluate the long-term safety of glatiramer acetate and its effect on the neurologic course of participants with relapsing-remitting multiple sclerosis (RRMS). Participants have scheduled visits every 3 months to assess glatiramer acetate safety and their Multiple Sclerosis (MS) status.

Timeline

Start
1994-03-26
Primary completion
2018-02-28
Completion
2018-02-28

Drugs

EvaluationDrugModalityDoseRoute
Subject Glatiramer Acetate Small molecule 20 mg Subcutaneous
Subject Glatiramer Acetate Small molecule 40 mg Subcutaneous