Her's a link to Synthon's PIII trial presumably needed for European approval:
Efficacy and Safety of GTR in Comparison to Copaxone® (GATE) This study is currently recruiting participants. Verified on December 2011 by Synthon BV
First Received on December 8, 2011. No Changes Posted Sponsor: Synthon BV Information provided by (Responsible Party): Synthon BV ClinicalTrials.gov Identifier: NCT01489254
Purpose The purpose of this study is demonstrate that efficacy and safety of Synthon's glatiramer acetate (GTR) is equivalent to Copaxone® (Teva) in patients with relapsing remitting multiple sclerosis
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