Abstract
Riluzole is the only drug shown to slow the course of amyotrophic lateral sclerosis (ALS). Patients with ALS-associated dysphagia may have to discontinue riluzole therapy because of their inability to swallow the tablet formulation of the drug. An oral suspension of riluzole (Teglutik®) has recently been approved, which may allow patients with ALS-associated dysphagia to continue riluzole therapy for longer.
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Acknowledgments
The review was reviewed by: A.C. Calvo, University of Zaragoza, Zaragoza, Spain; P. Couratier, CHU de Limoges, Limoges, France; G. Laekeman, Katholieke Universiteit Leuven, Leuven, Belgium; F. Viader, CHU de Caen, Caen, France. During the peer review process, the manufacturer of riluzole oral suspension was also offered an opportunity to review this article. Changes resulting from comments received were made on the basis of scientific and editorial merit.
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The preparation of this review was not supported by any external funding.
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GM. Keating is a salaried employee of Adis/Springer, is responsible for the article content and declares no conflicts of interest.
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Keating, G.M. Riluzole oral suspension in amyotrophic lateral sclerosis: a guide to its use. Drugs Ther Perspect 32, 282–286 (2016). https://doi.org/10.1007/s40267-016-0312-7
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DOI: https://doi.org/10.1007/s40267-016-0312-7