Ethical use of off-label disease-modifying therapies for multiple sclerosis
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SAGE Publications Ltd
Abstract
Background: Off-label disease-modifying therapies (DMTs) for multiple sclerosis (MS) are used in at least 89 countries. There is a need for structured and transparent evidence-based guidelines to support clinical decision-making, pharmaceutical policies and reimbursement decisions for off-label DMTs. Objectives/Results: The authors put forward general principles for the ethical use of off-label DMTs for treating MS and a process to assess existing evidence and develop recommendations for their use. Conclusion: The principles and process are endorsed by the World Federation of Neurology (WFN), American Academy of Neurology (AAN), European Academy of Neurology (EAN), Americas Committee for Treatment and Research in Multiple Sclerosis (ACTRIMS), European Committee for Treatment and Research in Multiple Sclerosis (ECTRIMS), Middle-East North Africa Committee for Treatment and Research in Multiple Sclerosis (MENACTRIMS) and Pan-Asian Committee for Treatment and Research in Multiple Sclerosis (PACTRIMS), and we have regularly consulted with the Brain Health Unit, Mental Health and Substance Use Department at the World Health Organization (WHO). © The Author(s), 2021.
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Keywords
Access to treatment, Disease-modifying therapies, Guideline, Off-label treatment, Humans, Multiple sclerosis, Neurology, Off-label use, United states, Azathioprine, Cladribine, Cyclophosphamide, Fludarabine, Immunoglobulin, Leflunomide, Methotrexate, Minocycline, Mitoxantrone, Mycophenolate mofetil, Rituximab, Article, Ataxia, Drug industry, Drug safety, Expanded disability status scale, Health care industry, Human, Internuclear ophthalmoplegia, Medical practice, Mental health, Myelooptic neuropathy, Nuclear magnetic resonance imaging, Ophthalmoplegia, Paraplegia, Plasma exchange, Practice guideline, Quality of life, Systematic review, Vertigo, Western hemisphere, World health organization, Off label drug use