A critical evaluation of fenfluramine hydrochloride for the treatment of Dravet syndrome

Expert Rev Neurother. 2022 May;22(5):351-364. doi: 10.1080/14737175.2021.1877540. Epub 2021 Feb 26.

Abstract

Introduction: Dravet Syndrome (DS) is a severe developmental and epileptic encephalopathy. Fenfluramine recently demonstrated to be a highly efficacious and safe treatment option for DS patients. Fenfluramine has been recently approved by the FDA and EMA and is marketed as Fintepla®.

Areas covered: DS and the need for additional anticonvulsive treatment options is discussed. The results of three placebo-controlled phase III studies (1 with and 2 without stiripentol) and 2 open label (extension) studies are reviewed. All studies demonstrate a consistent and impressive seizure reduction, confirming the results of two smaller investigator-initiated trials. The mechanism of action of fenfluramine is discussed. Finally, the place of fenfluramine in the future treatment of DS is outlined.

Expert opinion: Fenfluramine has a potent anticonvulsive effect in DS. Although not yet fully elucidated, the anticonvulsive mechanism of fenfluramine seems to be mainly serotonergic. Fenfluramine is generally well tolerated. A dose reduction is necessary in combination with stiripentol. Considering new competitors, efficacy seems lower for cannabidiol and is comparable with stiripentol. Preclinical studies indicate a disease specific action and possible disease modification in DS. The latter would support the use of fenfluramine above its anticonvulsive effect and needs to be further elaborated.

Keywords: 5-HT receptor; Dravet syndrome; SCN1A; epileptic encephalopathy; fenfluramine; pharmacokinetic interaction; serotonin (5-HT); sigma 1; stiripentol; sudep.

MeSH terms

  • Anticonvulsants / therapeutic use
  • Epilepsies, Myoclonic* / drug therapy
  • Epileptic Syndromes
  • Fenfluramine / therapeutic use
  • Humans
  • Seizures / drug therapy
  • Spasms, Infantile* / drug therapy

Substances

  • Anticonvulsants
  • Fenfluramine

Supplementary concepts

  • CDKL5 deficiency disorder