Thursday December 14th 2017

24-Month Interim Results Of PANGAEA: A 5-Year Registry Study Evaluating Long-Term Safety, Efficacy And Pharmacoeconomic Data Of German Multiple…

CONCLUSIONS:The results of the 24 month interim-analysis of PANGAEA confirm the positive safety and efficacy profile of fingolimod shown in Phase III clinical trials, under real-world conditions.Study Supported by: Novartis Pharma GmbH, Nuremberg, GermanyDisclosure: Dr. Ziemssen has received personal compensation for activities with Almirall, Biogen Idec, Bayer, Genzyme Corporation, GlaxoSmithKline, Inc., MSD, Merck Serono, Novartis, Sanofi, Teva Neuroscience, and Synthon. Dr. Ziemssen has received research support from Bayer, Biogen Idec, Merck Serono, Novartis, Teva, and Sanofi. Dr. Diaz Lorente has received personal compensation for activities with Novartis as an employee. Dr. Fuchs has received personal compensation for activities with Novartis. Dr. Cornelissen has received personal co…

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24-Month Interim Results Of PANGAEA: A 5-Year Registry Study Evaluating Long-Term Safety, Efficacy And Pharmacoeconomic Data Of German Multiple…

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