Disease-modifying treatments for MS – a review of approved medications: STUDY
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Background and purpose:
There is still no curative treatment for multiple sclerosis (MS), but during the last 20 years eight different disease-modifying compounds have been approved for relapsing−remitting MS (RRMS).
A literature search was conducted on published randomized controlled phase III trials indexed in PubMed on the approved medications until 21 May 2015.
In this review the mode of action, documented treatment effects and side effects of the approved MS therapies are briefly discussed.
Based on current knowledge of risk−benefit of the approved MS medications, including factors influencing adherence, it is suggested that oral treatment with Tecfidera (dimethyl fumarate) or Aubagio (teriflunomide) should be preferred as a starting therapy amongst the first-line preparations for de novo RRMS. In the case of breakthrough disease on first-line therapy, or rapidly evolving severe RRMS, second-line therapy with Tysabri (natalizumab), Gilenya (fingolimod) or Campath (alemtuzumab) should be chosen based on careful risk−benefit stratification.
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