Overview A Study to Evaluate the Impact of Using Warm Compress Prior to Daily Injections of Copaxone® Status: Completed Trial end date: 2006-02-01 Target enrollment: Participant gender: Summary This study is designed to compare skin reactions with or without the use of warm compress prior to performing a Copaxone® injection. Phase: Phase 4 Details Lead Sponsor: Teva Neuroscience, Inc.Teva Pharmaceutical IndustriesTreatments: (T,G)-A-LGlatiramer Acetate