Thursday December 14th 2017

Subgroup and Sensitivity Analyses of the Primary Endpoint from the Peginterferon Beta-1a ADVANCE Study: A Pivotal Phase 3 Study in Patients with…

CONCLUSION: Peginterferon beta-1a Q2W and Q4W demonstrated consistent reductions in ARR versus placebo. Multiple sensitivity analyses corroborated the robustness of the primary endpoint in the ADVANCE study.Study Sponsored by: Biogen Idec Inc.Disclosure: Dr. Kieseier has received personal compensation for activities with Bayer Pharmaceuticals Corp., Schering AG, Biogen Idec, Merck Serono, Novartis, Roche Diagnostics Corp., Sanofi-Aventis Pharmaceuticals Inc., and Teva Neuroscience. Dr Kieseier has received research support from Bayer Schering, Biogen Idec, Merck Serono, and Teva Neuroscience. Dr. Arnold has received personal compensation for activities with Acorda Therapeutics, Bayer Pharmaceuticals Corporation, Biogen Idec, Coronado Biosciences, EMD Serono, Genentech Inc., Genzyme Corpora…

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Subgroup and Sensitivity Analyses of the Primary Endpoint from the Peginterferon Beta-1a ADVANCE Study: A Pivotal Phase 3 Study in Patients with…

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