Multiple Sclerosis

The past 2 decades have seen significant improvements in disease-modifying therapies (DMTs) for multiple sclerosis (MS), and with them a surge in prices in the cost of therapy with sales more than doubling just in the past few years. As a result, there has been a significant rise in the cost of care for patients with MS.
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Findings from an ongoing, phase 3 clinical trial involving patients with relapsing-remitting multiple sclerosis (MS) reveal that hematopoietic stem-cell transplantation (HSCT) may be a feasible treatment option for reversing disability associated with MS.
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Multiple sclerosis (MS) is the leading cause of irreversible neurologic disability in young women in the United States, and the second leading cause of neurologic disability in young men. In a series of debates at the 2016 American Academy of Neurology annual meeting, expert physicians addressed current and controversial issues in neuroscience, including the early aggressive treatment of patients with MS.

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In a phase 3, randomized clinical trial, natalizumab (Tysabri) failed to slow the progression of ambulatory disability unrelated to relapses (primary end point) in patients with secondary progressive multiple sclerosis (MS). Although patients who received nataliz­umab were less likely to have progression of ambulatory disability than those receiving placebo, the difference was not significant, according to the results presented at the 2016 American Academy of Neurology annual meeting.

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The monoclonal antibody ocreliz­umab was recently granted a breakthrough therapy designation by the FDA for the treatment of patients with primary progressive multiple sclerosis (PPMS).
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Ozanimod, an oral modulator of the sphingosine1-phosphate (S1P) receptor, was effective up to 72 weeks in a blinded extension of the phase 2/3 RADIANCE clinical trial that included patients with relapsing forms of multiple sclerosis (MS).
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Could stem-cell transplantation prove equally efficacious and more cost-effective than the currently available and expensive drugs for multiple sclerosis (MS)? Experts weighed in on this topic at ACTRIMS Forum 2016, a recent meeting of the Americas Committee for Treatment and Research in Multiple Sclerosis.
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A preliminary analysis of predictors of disease-modifying therapy (DMT) adherence, presented at the American Academy of Neurology 2015 annual meeting, reinforces the notion that patient–provider communication is of primary importance.
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With worsening symptoms and increasingly unpredictable attacks, the burden for patients with secondary-progressive multiple sclerosis (MS) is undeniable, and studies have shown that accumulating levels of disability experienced by patients with MS have a direct impact on their quality of life.
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A pragmatic review of literature has identified best practices for network meta-analyses (NMAs) of disease-modifying drugs for the treatment of relapsing-remitting multiple sclerosis (RRMS).
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