Claims for Patent: 11,826,343

Summary for Patent: 11,826,343

Title:	Compositions and methods for treating epilepsy, seizures and other conditions
Abstract:	Compositions are provided for the liquid oral administration of topiramate and its salts. The invention further provides methods for treating diseases and disorders using the compositions.
Inventor(s):	Yu-Hsing Tu, Ashok Perumal, Kalyan Kathala, Romona BHATTACHARYA
Assignee:	Tulex Pharmaceuticals Inc
Application Number:	US18/126,551
Patent Claims:	1. A direct dosing device consisting of a liquid pharmaceutical composition, wherein the liquid pharmaceutical composition consists of: (a) polyethylene glycol in an amount of about 40% w/v to about 70% w/v; (b) one or more preservatives selected from parabens, benzyl alcohol, benzoic acid, sorbic acid, sodium benzoate, and ascorbic acid; (c) glycerin in an amount of about 60% to about 70% w/v; (d) topiramate, or a pharmaceutically acceptable addition salt thereof, in an amount of about 25 mg/ml; (e) one or more sweeteners; and (f) optionally, a flavor component comprising one or more flavor compounds; wherein: the total amount of water present in the composition is 0.35% w/w or less; wherein the liquid pharmaceutical composition is ready-to-use without dilution and configured to be administered directly to a subject in need thereof; the liquid pharmaceutical composition does not contain any added water, aqueous acid or base; and the liquid pharmaceutical composition is a liquid for oral administration. 2. The direct dosing device of claim 1, wherein the direct dosing device is a measuring device with graduations. 3. The direct dosing device of claim 1, wherein the polyethylene glycol is present in an amount of about of about 45% w/v to about 55% w/v. 4. The direct dosing device of claim 1, wherein the polyethylene glycol has a molecular weight of about 300 to about 8000. 5. The direct dosing device of claim 4, wherein the polyethylene glycol has a molecular weight of about 400. 6. The direct dosing device of claim 1, wherein the one or more preservatives is present in an amount of about 0.01% w/v to about 3% w/v. 7. The direct dosing device of claim 1, wherein the one or more preservatives is present in an amount of about 1.2% w/v to about 2.5% w/v. 8. The direct dosing device of claim 1, wherein the one or more preservatives comprises one or more parabens. 9. The direct dosing device of claim 8, wherein the one or more parabens are methylparaben and propylparaben. 10. The direct dosing device of claim 1, wherein the glycerin is present in an amount of about 60% to about 65% w/v. 11. The direct dosing device of claim 1, wherein the topiramate is in the form of a free acid. 12. The direct dosing device of claim 1, wherein the direct dosing device contains from 25 mg to 400 mg of topiramate or a pharmaceutically acceptable addition salt thereof. 13. The direct dosing device of claim 1, wherein the one or more sweeteners are present in an amount of about 0.5% w/v to about 2% w/v. 14. The direct dosing device of claim 1, wherein the one or more sweeteners are selected from sucralose, aspartame, mannitol, sorbitol, xylitol, acesulfame, neotame, stevia, dextrose, saccharin sodium, fructose, high fructose corn syrup, maltodextrin, and sucrose. 15. The direct dosing device of claim 14, wherein the one or more sweeteners is sucralose. 16. The direct dosing device of claim 1, wherein the flavor component is present in an amount of about 0.1% w/v to about 0.5% w/v. 17. The direct dosing device of claim 16, wherein the flavor component is present in an amount of about 0.2% w/v. 18. The direct dosing device of claim 1, wherein the liquid pharmaceutical composition is stable for at least 24 months at 20-25° C. 19. The direct dosing device of claim 1, wherein the liquid pharmaceutical composition is stable for at least 24 months at controlled room temperature.