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Deflazacort in Duchenne muscular dystrophy: a profile of its use in the USA

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Abstract

Deflazacort (Emflaza™) is a derivative of prednisolone with immunomodulatory and anti-inflammatory properties. Overall, in the treatment of boys with Duchenne muscular dystrophy (DMD), deflazacort is as effective as prednisone, but may be better tolerated. In a randomized, double-blind, phase 3 trial in boys with DMD, deflazacort and prednisone both preserved muscle strength more effectively than placebo after 12 weeks of treatment, with improvements being maintained until study end at week 52. Both active treatments were also associated with improved motor function. In the real-word setting, treatment with corticosteroids for ≥ 1 year significantly delayed disease progression relative to no or < 1 month of corticosteroid treatment, with deflazacort showing some benefits over prednisone/prednisolone. Body weight gain-related events were less frequent with deflazacort than with prednisone, but stunted growth and the development of non-serious cataracts were more frequent.

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Acknowledgements

This article was reviewed by: R.C. Griggs, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA; E.C.W. Leung, Manitoba Institute of Child Health, and Department of Pediatrics and Child Health, University of Manitoba, Winnipeg, MB, Canada. During the peer review process, the marketing authorization holder of deflazacort 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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Correspondence to Katherine Ann Lyseng-Williamson.

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The preparation of this review was not supported by any external funding.

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K. McKeage and K. A. Lyseng-Williamson are employees of Adis/Springer, are responsible for the article content and declare no conflicts of interest. Additional information about this Adis Drug Q&A can be found at http://www.medengine.com/Redeem/B1BCF0602140FE49.

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McKeage, K., Lyseng-Williamson, K.A. Deflazacort in Duchenne muscular dystrophy: a profile of its use in the USA. Drugs Ther Perspect 34, 16–22 (2018). https://doi.org/10.1007/s40267-017-0466-y

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