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      Cost-Effectiveness Analysis of Ofatumumab for the Treatment of Relapsing-Remitting Multiple Sclerosis in Canada

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          Abstract

          Background

          Ofatumumab is a high-efficacy disease-modifying therapy (DMT) approved for first-line treatment of relapsing-remitting multiple sclerosis (RRMS) in Canada.

          Objective

          The aim of this study was to evaluate the cost effectiveness of ofatumumab from a Canadian healthcare system perspective.

          Methods

          A Markov cohort model was run over 65 years using annual cycles, 1.5% annual discount rate, and 100% treatment discontinuation at 10 years. The British Columbia database informed natural history transition probabilities. Treatment efficacy for DMTs were sourced from a network meta-analysis. Clinical trial data were used to estimate probabilities for treatment-related adverse events. Health utilities and costs were obtained from Canadian sources (if available) and the literature.

          Results

          Among first-line indicated therapies for RRMS, ofatumumab was dominant (more effective, lower costs) over teriflunomide, interferons, dimethyl fumarate, and ocrelizumab. Compared with glatiramer acetate and best supportive care, ofatumumab resulted in incremental cost-effectiveness ratios (ICERs) of $24,189 Canadian dollars per quality-adjusted life-year (QALY) and $28,014/QALY, respectively. At a willingness-to-pay threshold of $50,000/QALY, ofatumumab had a 64.3% probability of being cost effective. Among second-line therapies (scenario analysis), ofatumumab dominated natalizumab and fingolimod and resulted in an ICER of $50,969 versus cladribine.

          Conclusions

          Ofatumumab is cost effective against all comparators and dominant against all currently approved and reimbursed first-line DMTs for RRMS, except glatiramer acetate.

          Supplementary Information

          The online version contains supplementary material available at 10.1007/s41669-022-00363-1.

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          Most cited references25

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          Ocrelizumab versus Interferon Beta-1a in Relapsing Multiple Sclerosis

          B cells influence the pathogenesis of multiple sclerosis. Ocrelizumab is a humanized monoclonal antibody that selectively depletes CD20+ B cells.
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            Ofatumumab versus Teriflunomide in Multiple Sclerosis

            Ofatumumab, a subcutaneous anti-CD20 monoclonal antibody, selectively depletes B cells. Teriflunomide, an oral inhibitor of pyrimidine synthesis, reduces T-cell and B-cell activation. The relative effects of these two drugs in patients with multiple sclerosis are not known.
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              ECTRIMS/EAN Guideline on the pharmacological treatment of people with multiple sclerosis

              Multiple sclerosis (MS) is a complex disease with new drugs becoming available in the past years. There is a need for a reference tool compiling current data to aid professionals in treatment decisions.
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                Author and article information

                Contributors
                soukaina.mouallif@novartis.com
                Journal
                Pharmacoecon Open
                Pharmacoecon Open
                PharmacoEconomics Open
                Springer International Publishing (Cham )
                2509-4262
                2509-4254
                15 September 2022
                15 September 2022
                November 2022
                : 6
                : 6
                : 859-870
                Affiliations
                [1 ]GRID grid.410356.5, ISNI 0000 0004 1936 8331, Department of Medicine, , Queen’s University, ; Kingston, ON Canada
                [2 ]GRID grid.17091.3e, ISNI 0000 0001 2288 9830, Department of Medicine, , The University of British Columbia, ; Vancouver, BC Canada
                [3 ]GRID grid.25055.37, ISNI 0000 0000 9130 6822, Department of Neurology, , Memorial University of Newfoundland, ; St. John’s, NL Canada
                [4 ]GRID grid.512384.9, EVERSANA, ; Burlington, ON Canada
                [5 ]Novartis Canada Inc., 385, boulevard Bouchard, Dorval, QC H9S 1A9 Canada
                [6 ]GRID grid.419481.1, ISNI 0000 0001 1515 9979, Novartis Pharma AG, ; Basel, Switzerland
                [7 ]Novartis Ireland Limited, Dublin, Ireland
                Article
                363
                10.1007/s41669-022-00363-1
                9596641
                36107307
                a2ea3cbc-b7ff-495b-b88b-e08a6d25b09d
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, which permits any non-commercial use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by-nc/4.0/.

                History
                : 7 August 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100009009, Novartis Pharmaceuticals Canada;
                Categories
                Original Research Article
                Custom metadata
                © The Author(s) 2022

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