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Comprehensive Autopsy Program for Individuals with Multiple Sclerosis
Published on: July 19, 2019
Dimethyl fumarate and teriflunomide for multiple sclerosis in a real-life setting: a French retrospective cohort
S Condé1, X Moisset1,2, B Pereira3
1Service de Neurologie, CHU Clermont-Ferrand, Université Clermont Auvergne, Clermont-Ferrand, France.
Background And Purpose:
Dimethyl fumarate (DMF) and teriflunomide are approved oral disease-modifying treatments for relapsing-remitting multiple sclerosis (MS). Phase 3 trials established these agents to be effective and generally well tolerated, although comparative efficacy and discontinuation rates are still unknown. The aim of this study was to assess real-world efficacy and discontinuation of DMF and teriflunomide in patients with relapsing-remitting MS.
Methods:
This retrospective observational cohort study was carried out in a French administrative region between March 2014 and July 2017. Patients who were followed by private or hospital neurologists were included. Efficacy and tolerance of the two treatments were assessed and compared by multivariate analysis, considering the duration of MS, annualized relapse rate and Expanded Disability Status Scale score at treatment initiation, treatment duration, type of prescriber and tobacco use.
Results:
We identified 189 DMF- and 157 teriflunomide-treated patients who had been treated for 22 ± 10 months. After correction for confounders, DMF more efficiently reduced the annualized relapse rate after 2 years than teriflunomide (0.06 vs. 0.21; P = 0.03). DMF-treated patients had more clinical and biological adverse events, resulting in a higher rate of treatment discontinuation (28% vs. 12%, P = 0.03).
Conclusion:
In this retrospective cohort study, DMF demonstrated significantly better efficacy over 2 years than teriflunomide, but tolerance to teriflunomide was better.
Insights
Dimethyl fumarate (DMF) shows better efficacy in reducing relapsing-remitting multiple sclerosis (MS) relapses over two years compared to teriflunomide. However, teriflunomide offers better treatment tolerance with lower discontinuation rates.
Area of Science:
- Neurology
- Immunology
- Pharmacology
Background:
- Dimethyl fumarate (DMF) and teriflunomide are oral disease-modifying treatments for relapsing-remitting multiple sclerosis (MS).
- While Phase 3 trials established their efficacy and tolerability, comparative real-world data on effectiveness and discontinuation rates remain limited.
Purpose of the Study:
- To assess and compare the real-world efficacy and discontinuation rates of DMF and teriflunomide in patients with relapsing-remitting MS.
Main Methods:
- A retrospective observational cohort study conducted in a French region from March 2014 to July 2017.
- Compared 189 DMF-treated patients and 157 teriflunomide-treated patients using multivariate analysis, adjusting for factors like MS duration, baseline relapse rate, and disability score.
Main Results:
- After adjusting for confounders, DMF significantly reduced the annualized relapse rate over two years compared to teriflunomide (0.06 vs. 0.21, P=0.03).
- DMF-treated patients experienced more clinical and biological adverse events, leading to higher discontinuation rates (28% vs. 12%, P=0.03).
Conclusions:
- Dimethyl fumarate (DMF) demonstrates superior efficacy in reducing MS relapses over two years compared to teriflunomide.
- Teriflunomide exhibits better treatment tolerance, resulting in lower discontinuation rates in a real-world setting.
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