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Rituximab in relapsing-remitting multiple sclerosis: A 72-week, open-label, phase I trial

โœ Scribed by Amit Bar-Or; Peter A. J. Calabresi; Douglas Arnold; Clyde Markowitz; Stuart Shafer; Lloyd H. Kasper; Emmanuelle Waubant; Suzanne Gazda; Robert J. Fox; Michael Panzara; Neena Sarkar; Sunil Agarwal; Craig H. Smith


Book ID
101466620
Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
171 KB
Volume
63
Category
Article
ISSN
0364-5134

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โœฆ Synopsis


Abstract

We evaluated the safety, tolerability, pharmacodynamics, and activity of Bโ€cell depletion with rituximab in patients with relapsingโ€remitting multiple sclerosis, receiving two courses of rituximab 6 months apart, and followed for a total of 72 weeks. No serious adverse events were noted; events were limited to mildโ€toโ€moderate infusionโ€associated events, which tended to decrease with subsequent infusions. Infections were also mild or moderate, and none led to withdrawal. Fewer new gadoliniumโ€enhancing or T2 lesions were seen starting from week 4 and through week 72. An apparent reduction in relapses was also observed over the 72 weeks compared with the year before therapy. Ann Neurol 2008


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Ocrelizumab in relapsing-remitting multi
โœ Ludwig Kappos; David Li; Peter A Calabresi; Paul O'Connor; Amit Bar-Or; Frederik ๐Ÿ“‚ Article ๐Ÿ“… 2011 ๐Ÿ› The Lancet ๐ŸŒ English โš– 337 KB

## Background: B lymphocytes are implicated in the pathogenesis of multiple sclerosis. we aimed to assess efficacy and safety of two dose regimens of the humanised anti-cd20 monoclonal antibody ocrelizumab in patients with relapsing-remitting multiple sclerosis. ## Methods: We did a multicentre,