Clinical and radiological outcomes of directed treatment transitions from Gilenya ® to generic fingolimod

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Authors: Mahi A. Patel, Tom G. Punnen, Kevin Shan, Morgan McCreary, Crystal Wright, Shanan B. Munoz, Paula Hardeman, Katy W. Burgess, Benjamin M. Greenberg, Lindsay A Horton, Peter V. Sguigna, Lauren M. Tardo
+2 more Olaf Stüve, Darin T. Okuda
Cited by: 1
References: 24

Abstract

Background: Gilenya ® (fingolimod), a sphingosine-1-receptor agonist, is an effective treatment for multiple sclerosis (MS). However, increased relapse activity has been observed after transitioning to generic fingolimod despite prior prolonged disease stability. Objective: To quantify the clinical and radiological impact of transitioning from Gilenya ® to generic fingolimod in people with MS (PwMS). Methods: Retrospective data were evaluated from a single tertiary MS care center. Time to magnetic resonance imaging (MRI) activity and clinical relapse was assessed during Gilenya ® and generic fingolimod treatment. Differences in absolute lymphocyte count (ALC) and side effects were also measured by treatment group. Results: The cohort included 88 PwMS (71 female; 76 White, mean age when starting Gilenya ® was 39.6 years (standard deviation (SD) = 10.6 years), and mean age when starting generic fingolimod was 46.9 years (SD = 11.2 years)). A shorter time to MRI activity ( p = 0.0026) and time to relapse ( p = 0.0027) was observed during generic fingolimod treatment. The ALC increased by 8.81% after generic fingolimod treatment, relative to Gilenya ® (95% CI = (2.00%, 16.08%), p = 0.01), with an intersubject variability of 1.97%. A 2.45-fold increase in side effects was observed with generic fingolimod relative to Gilenya ® (95% CI = (1.38, 4.36), p = 0.002). Conclusion: Measures of disease stability appear less optimal with generic fingolimod based on serological, clinical, and radiological measures.

Fields of Study & Subjects

Multiple Sclerosis Research Studies Peripheral Neuropathies and Disorders Sphingolipid Metabolism and Signaling

Publication details

Journal / source
Multiple Sclerosis Journal
Publisher
SAGE Publications
Volume
32
Issue
2
Pages
192–201
Publication date
3 January 2026
Language
EN