drugset / Trial / NCT00947752

Safety of New Formulation of Glatiramer Acetate

NCT00947752

Phase 3 Completed 147 enrolled Teva Branded Pharmaceutical Products R&D, Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to compare pain associated with injections and injection-site reactions of the approved formulation of Glatiramer Acetate (GA) versus investigational formulation of GA. In addition, the investigators will evaluate the side effects of the two formulations of GA.

Timeline

Start
2009-07
Primary completion
2009-09
Completion
2009-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Glatiramer Acetate Small molecule 20 mg Subcutaneous