rate (ARR) and disability progression. Objective: This phase 3, rater-blinded study
(NCT00883337) compared teriflunomide with interferon-beta-1a (IFNβ-1a). Methods:
Patients with relapsing multiple sclerosis were randomised (1: 1: 1) to oral teriflunomide 7-or
14mg, or subcutaneous IFNβ-1a 44µg. The primary composite endpoint was time to failure,
defined as first occurrence of confirmed relapse or permanent treatment discontinuation for …