Claims for Patent: 11,883,374

Summary for Patent: 11,883,374

Title:	Lacosamide pharmaceutical composition and dosage form thereof
Abstract:	A dosage form of lacosamide and a pharmaceutical dosage form thereof is disclosed. The dosage form includes an extended release portion and optionally an immediate release portion. Also provided are methods of providing extended release of lacosamide and treatment of a neurological or psychiatric disease or condition.
Inventor(s):	Shaoqiong Lyu, Shoufeng Li, Xun Zheng, Zhongqin WANG
Assignee:	Shanghai Aucta Pharmaceuticals Co Ltd
Application Number:	US17/664,513
Patent Claims:	1. A dosage form of lacosamide or a pharmaceutically acceptable salt thereof, comprising: (a) a first plurality of the particulates, each comprising i. a core comprising lacosamide or a pharmaceutically acceptable salt thereof, and ii. an extended release layer enclosing the core, wherein the extended release layer is free from lacosamide or a pharmaceutically acceptable salt thereof and comprises an extended release agent which is pH independent; wherein the core is free from the extended release agent, and (b) an immediate release portion of lacosamide or a pharmaceutically acceptable salt thereof in the form of a second plurality of particulates, wherein the lacosamide or the pharmaceutically acceptable salt thereof of the immediate release portion ranges from about 5% to about 30% by weigh in the total amount of the lacosamide or the pharmaceutically acceptable salt thereof in the dosage form, wherein the dosage form is configured to have an in-vitro dissolution according to the following: (a) less than about 20% in 1 hour; (b) about 20%-80% in 4 hours; and (c) more than about 80% in 12 hours; wherein the dissolution is determined using a USP type 1 dissolution system (Basket Apparatus) at 100 rpm and a temperature of 37±0.5° C. in 900 ml of pH 6.8 phosphate buffer for 12 hours. 2. The dosage form of claim 1, wherein the core comprises an inert inner core and an outer layer enclosing the inner core, and the lacosamide or a pharmaceutically acceptable salt thereof in (a) is disposed in the outer layer of the core. 3. The dosage form of claim 1, wherein lacosamide or a pharmaceutically acceptable salt thereof in the dosage form has an in-vitro dissolution according to the following: (a) from about 11% to about 18% in 1 hour, (b) from about 20% to about 35% in 2 hours, (c) from about 40% to about 70% in 4 hours, (d) from about 65% to about 95% in 6 hours, and (e) more than about 90% in 12 hours, wherein the in-vitro dissolution is determined using a USP type 1 dissolution system (Basket Apparatus) at 100 rpm and a temperature of 37±0.5° C. in 900 ml of pH 6.8 phosphate buffer for 12 hours. 4. The dosage form of claim 1, wherein the amount of lacosamide or a pharmaceutically acceptable salt thereof dissolved in the first two hours is about 1.5-2.0 times more than the amount dissolved in the first one hour, and the amount of lacosamide or a pharmaceutically acceptable salt thereof dissolved in the first four hours is about 1.7-2.2 times more than the amount dissolved in the first two hours, and the amount of lacosamide or a pharmaceutically acceptable salt thereof dissolved in the first six hours is about 1.7-2.2 times more than the amount dissolved in the first three hours. 5. The dosage form of claim 4, wherein the amount of lacosamide or a pharmaceutically acceptable salt thereof dissolved by 6th hour ranges from about 72% to about 90% of the total amount of lacosamide or a pharmaceutically acceptable salt thereof in the dosage form. 6. The dosage form of claim 1, wherein the total amount of lacosamide or a pharmaceutically acceptable salt thereof ranges from about 40% to about 80% by weight in the dosage form. 7. The dosage form of claim 1, wherein the extended release agent ranges from about 5% to about 30% by weight in the extended release portion. 8. The dosage form of claim 1, wherein a ratio between the lacosamide or a pharmaceutically acceptable salt thereof in the first plurality of the particulates and the extended release agent ranges from about 15:1 to about 1:1. 9. The dosage form of claim 1, wherein the total amount of lacosamide or a pharmaceutically acceptable salt thereof in the dosage form ranges from about 20 mg to about 600 mg. 10. The dosage form of claim 1, wherein the pH independent extended release agent is selected from the group consisting of ethyl cellulose, methyl cellulose, cellulose acetate, polyvinyl acetate, ethyl acrylate/methyl methacrylate/trimethylamino ethyl methacrylate chloride copolymer, ethyl acrylate/methyl methacrylate/trimethylamino ethyl methacrylate chloride copolymer, and any mixtures thereof. 11. The dosage form of claim 1, wherein the pH independent extended release agent is ethyl cellulose. 12. The dosage form of claim 1, wherein the dosage form contains lacosamide only in salt free form, and wherein the lacosamide of the immediate release portion ranges from about 5% to about 15% by weigh in the total amount of lacosamide in the dosage form. 13. The dosage form of claim 1, where the first plurality of particulates have an average diameter ranging from about 300 μm to about 1400 μm. 14. The dosage form of claim 1, wherein the dosage form when orally administered once daily achieves more than 90% of the AUC(0-inf) of an immediate released reference lacosamide administered to the subject in fasting condition, wherein the daily dosage of the dosage form is the same as the daily dosage of the immediate released reference lacosamide. 15. A method of providing an extended release of lacosamide in a subject, comprising administering to the subject a dosage form of claim 1, wherein the amount of the lacosamide or the pharmaceutically acceptable salt thereof and the amount of the pH independent extended release agent are selected so that the dosage form provides an in-vitro dissolution according the following: (a) from about 11% to about 18% in 1 hour, (b) from about 20% to about 35% in 2 hours, (c) from about 40% to about 70% in 4 hours, (d) from about 65% to about 95% in 6 hours, and (e) more than about 90% in 12 hours, wherein the in-vitro dissolution is determined using a USP type 1 dissolution system (Basket Apparatus) at 100 rpm and a temperature of 37±0.5° C. in 900 ml of pH 6.8 phosphate buffer for 12 hours. 16. The method of claim 15, wherein the dosage from is administered once a day. 17. A method of treating a neurological or psychiatric disease or condition, comprising administering to a subject in need thereof a dosage of claim 1. 18. The method of claim 17, wherein the disease or condition is selected from the group consisting of epilepsy, migraine, essential tremor, restless limb syndrome, cluster headache, neuralgia, neuropathic pain, Tourette's syndrome, infantile spasm, anxiety, bipolar disorder, psychosis, mania, schizophrenia, depression, dementia, autism, obsessive compulsive disorder, post-traumatic stress disorder, attention deficit hyperactivity disorder, impulse control disorder, borderline personality disorder, addiction, chronic neurodegenerative disorder, acute neurodegeneration, and amyotrophic lateral sclerosis. 19. The method of claim 17, wherein the disease or condition is epilepsy.