Claims for Patent: 12,097,206

Summary for Patent: 12,097,206

Title:	Method for the treatment of Dravet Syndrome
Abstract:	A method of treating and/or preventing Dravet Syndrome in a patient such as a patient previously diagnosed with Dravet Syndrome, by administering an effective dose of fenfluramine or its pharmaceutically acceptable salt to that patient. Dravet Syndrome patients are typically children under the age of 18 and are treated at a preferred dose of less than about 0.5 to about 0.01 mg/kg/day.
Inventor(s):	Berten Ceulemens, Lieven Lagae
Assignee:	UNIVERSITY HOSPITAL ANTWERP , Katholieke Universiteit Leuven
Application Number:	US17/667,136
Patent Claims:	1. A method of adjunctive treating, preventing and/or ameliorating seizures in a patient diagnosed with Dravet syndrome, comprising: administering to the patient an effective dose of fenfluramine or a pharmaceutically acceptable salt thereof in a dose of 0.2 mg/kg/day to 0.5 mg/kg/day to the patient; administering to the patient an effective dose of stiripentol or a pharmaceutically acceptable salt thereof; and administering to the patient an effective dose of clobazam or a pharmaceutically acceptable salt thereof; and whereby seizures are ameliorated in the patient. 2. A method of adjunctive treating, preventing and/or ameliorating seizures in a patient diagnosed with Dravet syndrome and not responsive to prior treatment, comprising: administering to the patient an effective dose of fenfluramine or a pharmaceutically acceptable salt thereof in a dose of 0.5 mg/kg/day to 0.2 mg/kg/day to the patient; administering to the patient an effective dose of stiripentol or a pharmaceutically acceptable salt thereof; and administering to the patient an effective dose of clobazam or a pharmaceutically acceptable salt thereof; and whereby seizures are ameliorated in the patient not responsive to prior treatment. 3. The method of claim 2, wherein the patient is shown to have a genetic mutation selected from the group consisting of SCN1A, SCN1B, SCN2A, SCN3A, SCN9A, GABRG2, GABRD and PCDH19. 4. A method of adjunctive treating, preventing and/or ameliorating seizures, comprising: determining a patient has a mutation in a gene which mutation is associated with Dravet syndrome; administering to the patient determined to have the mutation: (a) 0.2 mg/kg/day of fenfluramine or a pharmaceutically acceptable salt thereof; (b) an effective dose of stiripentol or a pharmaceutically acceptable salt thereof; and (c) an effective dose of clobazam or a pharmaceutically acceptable salt thereof; whereby seizures are ameliorated in the patient exhibiting the mutation. 5. The method as claimed in claim 4, wherein the mutation is selected from the group consisting of SCN1A, SCN1B, SCN2A, SCN3A, SCN9A, GABRG2, GABRD and PCDH19.