COVID-19 Infection in Fingolimod- or Siponimod-Treated Patients: Case Series

Roseanne Sullivan1, Ajay Kilaru2, Bernhard Hemmer2

  • 1From the Novartis Pharmaceuticals Corporation (R.S.), East Hanover, NJ; Novartis Pharma AG (A.K., T.H., V.D.), Basel, Switzerland; Department of Neurology, Technical University of Munich, and Munich Cluster for Systems Neurology (SyNergy) (B.H.), Germany; Weill Institute for Neurosciences (B.A.C.C.), Department of Neurology, University of California San Francisco, CA; Department of Neurology (B.M.G.), University of Texas Southwestern, Dallas, TX; Novartis Healthcare Pvt. Ltd. (U.K.), Hyderabad, India; Department of Medicine (B.J.W.), Division of Experimental Medicine, Research Institute of the McGill University Health Centre, Montreal, Canada; and Department of Neurology (J.B.), Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA. roseanne.sullivan@novartis.com.

Summary

COVID-19 outcomes in patients with multiple sclerosis (MS) on fingolimod or siponimod appear similar to the general population. However, data limitations from spontaneous reporting require careful interpretation of these findings.

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