This year marks the 25th anniversary of the publication of the Betaseron phase III study (Interferon-beta MS Study Group. Neurology 1993;43:655-661), which ushered in the era of disease-modifying therapies in the treatment of multiple sclerosis. In the usual course of things, first-generation agents – especially drugs administered by injection – would be superseded by novel therapies, either a more convenient oral agent (fingolimod, teriflunomide, dimethyl fumarate, cladribine) or a more potent infusion drug (natalizumab, alemtuzumab, ocrelizumab). Market shares have shifted but all treatments remain available, resulting in the present state of a surprisingly lengthy list of options. This raises the questions: are so many medications needed, and what is the role of injectable agents in MS management? Read More
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Update on CGRP inhibitors in migraine
May 18, 2018SPECIAL REPORT
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Calcitonin gene-related peptide (CGRP) inhibitors are emerging as an important class of agents for the prevention of episodic and chronic migraine (See Targeting CGRP in migraine, NeuroSens, March 28, 2018). Four monoclonal antibodies are currently in development: erenumab, a fully-human MAb targeting the CGRP receptor; and three humanized MAbs targeting the CGRP ligand (fremanezumab, eptinezumab, galcanezumab). Erenumab received FDA approval for the treatment of migraine this week. Read More
Update on oral cladribine – Effect on lymphocytes and safety data
May 9, 2018SPECIAL REPORT
New data were presented at the American Academy of Neurology annual meeting on the effect of oral cladribine on lymphocyte subsets in relapsing multiple sclerosis, providing new insights for evaluating the safety and efficacy of the drug. Oral cladribine is a cell-depleting disease-modifying drug, which was approved for use in Canada in November 2017. Read More
AAN 2018 DAILY REPORT
April 26, 2018Report from the American Academy of Neurology annual meeting, Los Angeles, April 21-27, 2018
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