Claims for Patent: 10,603,290

Summary for Patent: 10,603,290

Title:	Formulation for inhibiting formation of 5-HT.sub.2B agonists and methods of using same
Abstract:	Drug combinations and their use are disclosed. A first drug is administered in combination with a second drug. The first drug such as fenfluramine is characterized by the formation of a metabolite including 5-HT.sub.2B agonists such as norfenfluramine with known adverse side effects. The second drug is in the form of a CYP inhibitor such as cannabidiol which modulates the formation of metabolite down thereby making the first drug safer.
Inventor(s):	Farr; Stephen J. (Orinda, CA), Boyd; Brooks (Berkeley, CA)
Assignee:	ZOGENIX INTERNATIONAL LIMITED (Berkshire, GB)
Application Number:	16/193,812
Patent Claims:	1. A method of reducing or ameliorating seizures in a patient, comprising: administering fenfluramine; and administering cannabidiol thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine. 2. The method of claim 1, wherein the patient is diagnosed with Dravet syndrome. 3. The method of claim 1, wherein the patient is diagnosed with a form of refractory epilepsy selected from the group consisting of Dravet syndrome, Lennox-Gastaut syndrome, Doose syndrome, and West syndrome. 4. The method of claim 1, further comprising: co-administering to the subject an effective amount of a co-therapeutic agent selected from the group consisting of acetazolamide, barbexaclone, beclamide, brivaracetam, buproprion, cinacalet, clobazam, clonazepam, clorazepate, diazepam, divaloprex, eslicarbazepine acetate, ethadione, ethotoin, felbamate, gabapentin, lacosamide, lorazepam, mephenytoin, methazolamide, methsuximide, methylphenobarbitol, midazolam, nimetazepam, nitrazepam, oxcarbazepine, paramethadione, perampanel, piracetam, phenacemide, pheneturide, phensuximide, phenytoin, potassium bromide, pregabalin, primidone, retigabine, rufinamide, selectracetam, sodium valproate, stiripentol, sultiame, temazepam, tiagabine, topiramate, trimethadione, valnoctamide, valpromide, vigabatrin, zonisamide, and pharmaceutically acceptable salts thereof. 5. A method of reducing or ameliorating seizures in a patient diagnosed with a form of refractory epilepsy, comprising: administering a liquid formulation of fenfluramine to the patient in an amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day; and administering cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine. 6. A method of reducing or ameliorating seizures in a patient diagnosed with a form of refractory epilepsy, comprising: administering a liquid formulation of fenfluramine to the patient in an amount which is 30% less than an effective amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day, due to co-administration of cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine. 7. The method of claim 6, wherein the fenfluramine is administered in an amount of 70% less than an effective dose of 0.8 mg/kg/day. 8. The method of claim 6, wherein the fenfluramine is administered in an amount of 0.56 mg/kg/day or less. 9. A method of reducing or ameliorating seizures patient diagnosed with Dravet syndrome, comprising: administering a liquid formulation of fenfluramine to the patient in an amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day; and administering cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine. 10. A method of reducing or ameliorating seizures in a patient diagnosed with Dravet syndrome, comprising: administering a liquid formulation of fenfluramine to the patient in an amount which is 40% less than an effective amount in the range of 0.2 mg/kg/day to 0.8 mg/kg/day, due to co-administration of cannabidiol in a liquid formulation in an amount of 0.5 mg/kg/day to 25 mg/kg/day thereby modulating down formation of norfenfluramine, and resulting in higher levels of fenfluramine.