drugset / Trial / NCT01874145

Safety and Tolerability of Glatiramer Acetate

NCT01874145

Phase 3 Completed 209 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedParallel-groupOpen-labelTreatment

Summary

This is an open-label, randomized, multi-center, parallel-arm study to assess the safety and tolerability of a daily dose of Glatiramer Acetate (GA) 40 mg/mL three times a week (TIW) administered subcutaneously (SC) as compared to GA 20 mg/mL every day (QD) administered SC.

Timeline

Start
2013-06
Primary completion
2014-04
Completion
2014-05

Drugs

EvaluationDrugModalityDoseRoute
Comparator Glatiramer Acetate Small molecule 20 mg/ml Subcutaneous
Comparator Glatiramer Acetate Small molecule 40 mg/ml Subcutaneous