Fenfluramine HCl (Fintepla


Journal

Epilepsia
ISSN: 1528-1167
Titre abrégé: Epilepsia
Pays: United States
ID NLM: 2983306R

Informations de publication

Date de publication:
11 2020
Historique:
received: 15 05 2020
revised: 18 09 2020
accepted: 22 09 2020
pubmed: 21 10 2020
medline: 4 2 2021
entrez: 20 10 2020
Statut: ppublish

Résumé

Fenfluramine has been shown to provide clinically meaningful and statistically significant reductions in convulsive seizure frequency in children and adolescents (aged 2-18 years) with Dravet syndrome in two randomized, placebo-controlled clinical trials. The objective of this analysis was to assess longer-term safety and efficacy of fenfluramine in patients who completed one of the double-blind studies and entered an open-label extension (OLE) study. Patients enrolling in the OLE study initiated fenfluramine at 0.2 mg/kg/d regardless of their treatment assignment in the double-blind study. After 4 weeks, the fenfluramine dose could be titrated based on efficacy and tolerability to maximum of 0.7 mg/kg/d (absolute maximum 27 mg/d) or maximum of 0.4 mg/kg/d (absolute maximum 17 mg/d) in patients receiving concomitant stiripentol. The number and type of seizures were recorded daily in an electronic diary, and safety, including echocardiography, was assessed at Months 1, 2, and 3, and at 3-month intervals thereafter. A total of 232 patients were enrolled as of March 13, 2018. During this analysis period, patients were treated for a median 256 days (range = 46-634 days). Over the entire OLE analysis period, the median decrease in convulsive seizure frequency compared to baseline in the double-blind studies was -66.8% (range = -100% to 234.9%; P < .001). The median reduction in seizure frequency was similar in patients <6 (-75.7%) and ≥6 years old (-64.7%). The most commonly reported adverse events included pyrexia (21.6%), nasopharyngitis (19.4%), and decreased appetite (-15.9%). No valvular heart disease (VHD) or pulmonary arterial hypertension (PAH) was observed. Study results demonstrate that fenfluramine provides clinically meaningful (≥50%) seizure frequency reduction over an extended period in patients with Dravet syndrome. No patient developed VHD or PAH, and fenfluramine was generally well tolerated.

Identifiants

pubmed: 33078386
doi: 10.1111/epi.16722
pmc: PMC7756901
doi:

Substances chimiques

Serotonin Uptake Inhibitors 0
Fenfluramine 2DS058H2CF

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2396-2404

Informations de copyright

© 2020 Zogneix Inc. Epilepsia published by Wiley Periodicals LLC on behalf of International League Against Epilepsy.

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Auteurs

Joseph Sullivan (J)

Benioff Children's Hospital, University of California San Francisco, San Francisco, CA, USA.

Ingrid E Scheffer (IE)

Austin Health and Royal Children's Hospital, University of Melbourne, Melbourne, VIC, Australia.

Lieven Lagae (L)

Department of Paediatric Neurology, University of Leuven, Leuven, Belgium.

Rima Nabbout (R)

Service de Neurologie Pédiatrique Centre de Référence Épilepsies Rares (CReER), Hôpital Universitaire Necker - Enfants Malades, Paris, France.

Milka Pringsheim (M)

Department of Pediatric Cardiology, German Heart Centre Munich, Munich, Germany.
Pediatric Neurology, Schön Klinik Vogtareuth, Vogtareuth, Germany.

Dinesh Talwar (D)

Center for Neurosciences, University of Arizona Health Sciences Center, Tucson, AZ, USA.

Tilman Polster (T)

Department of Pediatric Epileptology, Bethel Epilepsy Center, Mara Hospital, Bielefeld, Germany.

Bradley Galer (B)

Zogenix, Inc, Emeryville, CA, USA.

Michael Lock (M)

Zogenix, Inc, Emeryville, CA, USA.

Anupam Agarwal (A)

Zogenix, Inc, Emeryville, CA, USA.

Arnold Gammaitoni (A)

Zogenix, Inc, Emeryville, CA, USA.

Glenn Morrison (G)

Zogenix, Inc, Emeryville, CA, USA.

Gail Farfel (G)

Zogenix, Inc, Emeryville, CA, USA.

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Classifications MeSH