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Butzkueven H, Belachew S, Kappos L et al. Baseline characteristics, treatment efficacy, and serious adverse events in natalizumab-treated MS patients without prior treatment. F1000Posters 2012, 3:862 (poster)

Baseline characteristics, treatment efficacy, and serious adverse events in natalizumab-treated MS patients without prior treatment

Helmut Butzkueven1, Shibeshih Belachew, Ludwig Kappos, Fabio Pellegrini, Maria Trojano, Heinz Wiendl, Annie Zhang, Ryan Arnold
Published 31 Jul 2012
Author Affiliations
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Published 31 Jul 2012

Baseline characteristics, treatment efficacy, and serious adverse events in natalizumab-treated MS patients without prior treatment

[version 1; not peer reviewed]

Helmut Butzkueven1, Shibeshih Belachew, Ludwig Kappos, Fabio Pellegrini, Maria Trojano, Heinz Wiendl, Annie Zhang, Ryan Arnold
Author Affiliations
1 Department of Medicine and Melbourne Brain Centre, Royal Melbourne Hospital, Australia
Presented at
22nd Meeting of the European Neurological Society 2012
Abstract
Competing Interests

Corresponding author Helmut Butzkueven is on the scientific advisory boards and receives travel support of Biogen Idec, Merck Serono, Novartis, sanofi-aventis. He has also been involved in the steering committees for trials conducted by Biogen Idec, Merck Serono, Novartis and received research support from Biogen Idec, Merck Serono, Novartis, as the honorary chair of the MSBase Foundation. Helmut is on the editorial board of Multiple Sclerosis International Federation and Multiple Sclerosis and Related Disorders, and is the current recipient of National Health and Medical Research Council (NHMRC)Career Development Award, NHMRC Project Grants, NHMRC Centre of Excellence Award, Australian Research Council Linkage Grant, and a National MS Society (USA) Project Grant.

Coauthor Shibeshih Belachew is a consultant for Bayer Schering, Biogen Idec, Merck Serono. Shibeshih also receives educational funding from Biogen Idec, Merck Serono, Novartis, sanofi-aventis, Teva.

Coauthor Ludwig Kappos has received payments as the principal investigator, member, or chair of planning and steering committees or advisory boards in corporate-sponsored clinical trials that have been sponsored by Actelion, Bayer HealthCare, Bayer Schering, Biogen Idec, BioMarin, CLC Behring, Elan, GeNeuro, Genmab, Genmark, GlaxoSmithKline, Lilly, Merck Serono, Novartis, Novonordisk, Peptimmune, sanofi-aventis, Santhera, Roche, Teva, UCB, and Wyeth. There has also been payments exclusively used for the funding of research at Ludwig's department with support coming from; Actelion, Bayer HealthCare, Bayer Schering, Biogen Idec, BioMarin, CLC Behring, Elan, Genmab, GeNeuro, Genmark, GlaxoSmithKline, Lilly, Merck Serono, Novartis, Novo Nordisk, Peptimmune, sanofi-aventis, Santhera, Roche, Teva, UCB, Wyeth. Ludwig has also received grants from the Swiss MS Society, the Swiss National Research Foundation, the European Union, the Gianni Rubatto, Novartis and Roche Research Foundations.

Coauthor Fabio Pellegrini receives honoraria and is also a consultant for Biogen Idec.

Coauthor Marie Trojano receives research support from Merck Serono and is a consultant/speaker honoraria for Bayer Schering, Biogen Idec, and sanofi-aventis.

Coauthor Heinz Wiendl receives honoraria from Bayer, Biogen Idec/Elan, Medac, Merck Serono, Novo Nordisk, sanofi-aventis, Schering, Teva. He also receives research support from Bayer, Biogen Idec/Elan, Merck Serono, Novo Nordisk, Medac, sanofi-aventis, Schering, Teva and is a consultant for BayerVital/Schering, Biogen Idec, Medac, Merck Serono, Novartis, Novo Nordisk, sanofi-aventis, Teva.

Coauthors Annie Zhang and Ryan Arnold are paid employees of Biogen Idec.

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