Claims for Patent: 10,695,336

Summary for Patent: 10,695,336

Title:	Dose-dumping resistant controlled release dosage form
Abstract:	The present invention provides a simple and improved dosage form that provides a controlled release of methylphenidate contained in the core thereof. The invention also provides methods of administering the dosage form and of treating conditions that are therapeutically responsive to methylphenidate. The dosage form exhibits improved resistance to alcohol-related dose dumping.
Inventor(s):	Hernan D. Benedetti, Cristian R. FRANCO, Guido S. BIGATTI, Joaquina Faour, Ana C. PASTINI
Assignee:	Acella Pharmaceuticals LLC
Application Number:	US16/269,126
Patent Claims:	1. A method of treating a condition that is therapeutically responsive to MPH or salt thereof, the method comprising orally administering at least one dosage form comprising an extended release composition comprising methylphenidate (MPH) or salt thereof, and a MPH-containing or MPH salt-containing rapid release or immediate release composition, wherein the extended release composition exhibits a less than 1.5-fold ethanol-related increase in the total amount of MPH or salt thereof released from the extended release composition during the first 120 minutes when comparing the MPH or salt thereof release rates in aqueous 0.1 N HCl at 37±1° C. and in 40% ethanol in aqueous 0.1 N HCl at 37±1° C., wherein, for the extended release composition, about 25% to about 35% wt of MPH or salt thereof is released by about 2 hours, about 45% to about 60% wt of MPH or salt thereof is released by about 4 hours, about 65% to about 85% of MPH or salt thereof is released by about 6 hours, about 85% to about 100% wt of MPH or salt thereof is released by about 8 hours and no less than 85% of MPH or salt thereof is released by about 10 hours after placement in aqueous 0.1 N HCl at 37±1° C., wherein the total dose of MPH or salt thereof in said at least one dosage form is about 54 mg, and said at least one dosage form provides a pharmacokinetic profile defined about as follows: Fed Fasted Standard Standard Parameter Mean deviation Mean deviation Tmax (h) 5.7 2.3 6 1 Cmax (ng/mL) 16 4.8 15 6 AUCinf (h*ng/mL) 180 54 180 82. 2. The method of claim 1, wherein the extended release composition exhibits a less than 2-fold ethanol-related increase in the average rate of MPH or salt thereof released from the extended release composition during the time period of 15 minutes to 120 minutes when comparing the release rates in aqueous 0.1 N HCl at 37±1° C. and in 40% ethanol in aqueous 0.1 N HCl at 37±1° C. 3. The method of claim 1, wherein the MPH or salt thereof is divided between the rapid release or immediate release composition and the extended release composition according to the following proportions: a) 1-40% wt in the rapid release or immediate release composition and 99-60% wt in the extended release composition; b) 10-40% wt in the rapid release or immediate release composition and 90-60% wt in the extended release composition; c) 15-35% wt in the rapid release or immediate release composition and 85-65% wt in the extended release composition; d) 15-25% wt in the rapid release or immediate release composition and 85-75% wt in the extended release composition; e) 15-20% wt in the rapid release or immediate release composition and 85-80% wt in the extended release composition; f) 20% wt or less in the rapid release or immediate release composition and 80% wt or more in the extended release composition; g) about 18% wt in the rapid release or immediate release composition and about 82% wt in the extended release composition; or h) about 22% wt in the rapid release or immediate release composition and about 78% wt in the extended release composition. 4. The method of claim 1, wherein the dosage form exhibits an in vitro release profile selected from any one of the following for the total amount of MPH or salt thereof released from the extended release composition and the rapid release or immediate release composition: Deionized water Deionized water Deionized water Dissolution Dissolution Dissolution Time (% wt) Median (% wt) Median (% wt) Median (hr) or mean range or mean range or mean range 1 20-30 22-27 21-27 2 25-35 29-33 27-34 4 45-60 51-57 46-57 6 68-85 74-83 68-83 8 90-100 97-100 92-100 10 91-100 99-100 95-100. 5. The method of claim 1, wherein the MPH salt is MPH hydrochloride. 6. The method of claim 1, wherein said pharmacokinetic profile is provided following oral administration of a single dosage form comprising said total dose. 7. The method of claim 1, wherein a single dosage form comprising said total dose is administered daily. 8. The method of claim 1, wherein the condition is selected from the group consisting of attention deficit hyperactivity disorder, narcolepsy, postural orthostatic tachycardia syndrome, lethargy, fatigue, bipolar disorder, lack of attention, opioid induced somnolence, major depressive disorder and obesity. 9. A method of treating a condition that is therapeutically responsive to MPH or salt thereof, the method comprising orally administering at least one dosage form comprising an extended release composition comprising methylphenidate (MPH) or salt thereof, and a MPH-containing or MPH salt-containing rapid release or immediate release composition, wherein the extended release composition exhibits a less than 1.5-fold ethanol-related increase in the total amount of MPH or salt thereof released from the extended release composition during the first 120 minutes when comparing the MPH or salt thereof release rates in aqueous 0.1 N HCl at 37±1° C. and in 40% ethanol in aqueous 0.1 N HCl at 37±1° C., wherein, for the extended release composition, about 25% to about 35% wt of MPH or salt thereof is released by about 2 hours, about 45% to about 60% wt of MPH or salt thereof is released by about 4 hours, about 65% to about 85% of MPH or salt thereof is released by about 6 hours, about 85% to about 100% wt of MPH or salt thereof is released by about 8 hours and no less than 85% of MPH or salt thereof is released by about 10 hours after placement in aqueous 0.1 N HCl at 37±1° C., wherein the total dose of MPH or salt thereof in said at least one dosage form is about 72 mg, and said at least one dosage form provides a pharmacokinetic profile defined about as follows: Fasted Standard Parameter Mean deviation Tmax (h) 5.68 0.96 Cmax (ng/mL) 20.6 6.24 AUCinf (h*ng/mL) 218.1 83.78. 10. The method of claim 9, wherein the extended release composition exhibits a less than 2-fold ethanol-related increase in the average rate of MPH or salt thereof released from the extended release composition during the time period of 15 minutes to 120 minutes when comparing the release rates in aqueous 0.1 N HCl at 37±1° C. and in 40% ethanol in aqueous 0.1 N HCl at 37±1° C. 11. The method of claim 9, wherein the MPH or salt thereof is divided between the rapid release or immediate release composition and the extended release composition according to the following proportions: a) 1-40% wt in the rapid release or immediate release composition and 99-60% wt in the extended release composition; b) 10-40% wt in the rapid release or immediate release composition and 90-60% wt in the extended release composition; c) 15-35% wt in the rapid release or immediate release composition and 85-65% wt in the extended release composition; d) 15-25% wt in the rapid release or immediate release composition and 85-75% wt in the extended release composition; e) 15-20% wt in the rapid release or immediate release composition and 85-80% wt in the extended release composition; f) 20% wt or less in the rapid release or immediate release composition and 80% wt or more in the extended release composition; g) about 18% wt in the rapid release or immediate release composition and about 82% wt in the extended release composition; or h) about 22% wt in the rapid release or immediate release composition and about 78% wt in the extended release composition. 12. The method of claim 9, wherein the dosage form exhibits an in vitro release profile selected from any one of the following for the total amount of MPH or salt thereof released from the extended release composition and the rapid release or immediate release composition: Deionized water Deionized water Deionized water Dissolution Dissolution Dissolution Time (% wt) Median (% wt) Median (% wt) Median (hr) or mean range or mean range or mean range 1 20-30 22-27 21-27 2 25-35 29-33 27-34 4 45-60 51-57 46-57 6 68-85 74-83 68-83 8 90-100 97-100 92-100 10 91-100 99-100 95-100. 13. The method of claim 9, wherein the MPH salt is MPH hydrochloride. 14. The method of claim 9, wherein said pharmacokinetic profile is provided following oral administration of a single dosage form comprising said total dose. 15. The method of claim 9, wherein a single dosage form comprising said total dose is administered daily. 16. The method of claim 9, wherein the condition is selected from the group consisting of attention deficit hyperactivity disorder, narcolepsy, postural orthostatic tachycardia syndrome, lethargy, fatigue, bipolar disorder, lack of attention, opioid induced somnolence, major depressive disorder and obesity. 17. A method of treating a condition that is therapeutically responsive to MPH or salt thereof, the method comprising orally administering at least one dosage form comprising an extended release composition comprising methylphenidate (MPH) or salt thereof, and a MPH-containing or MPH salt-containing rapid release or immediate release composition, wherein the extended release composition exhibits a less than 1.5-fold ethanol-related increase in the total amount of MPH or salt thereof released from the extended release composition during the first 120 minutes when comparing the MPH or salt thereof release rates in aqueous 0.1 N HCl at 37±1° C. and in 40% ethanol in aqueous 0.1 N HCl at 37±1° C., wherein, for the extended release composition, about 25% to about 35% wt of MPH or salt thereof is released by about 2 hours, about 45% to about 60% wt of MPH or salt thereof is released by about 4 hours, about 65% to about 85% of MPH or salt thereof is released by about 6 hours, about 85% to about 100% wt of MPH or salt thereof is released by about 8 hours and no less than 85% of MPH or salt thereof is released by about 10 hours after placement in aqueous 0.1 N HCl at 37±1° C., wherein the total dose of MPH or salt thereof in said at least one dosage form is about 2.5 mg to about 90 mg, and wherein the dosage form exhibits an in vitro release profile selected from any one of the following for the total amount of MPH or salt thereof released from the extended release composition and the rapid release or immediate release composition: Deionized water Deionized water Deionized water Dissolution Dissolution Dissolution Time (% wt) Median (% wt) Median (% wt) Median (hr) or mean range or mean range or mean range 1 20-30 22-27 21-27 2 25-35 29-33 27-34 4 45-60 51-57 46-57 6 68-85 74-83 68-83 8 90-100 97-100 92-100 10 91-100 99-100 95-100. 18. The method of claim 17, wherein the extended release composition exhibits a less than 2-fold ethanol-related increase in the average rate of MPH or salt thereof released from the extended release composition during the time period of 15 minutes to 120 minutes when comparing the release rates in aqueous 0.1 N HCl at 37±1° C. and in 40% ethanol in aqueous 0.1 N HCl at 37±1° C. 19. The method of claim 17, wherein the MPH or salt thereof is divided between the rapid release or immediate release composition and the extended release composition according to the following proportions: a) 1-40% wt in the rapid release or immediate release composition and 99-60% wt in the extended release composition; b) 10-40% wt in the rapid release or immediate release composition and 90-60% wt in the extended release composition; c) 15-35% wt in the rapid release or immediate release composition and 85-65% wt in the extended release composition; d) 15-25% wt in the rapid release or immediate release composition and 85-75% wt in the extended release composition; e) 15-20% wt in the rapid release or immediate release composition and 85-80% wt in the extended release composition; f) 20% wt or less in the rapid release or immediate release composition and 80% wt or more in the extended release composition; g) about 18% wt in the rapid release or immediate release composition and about 82% wt in the extended release composition; or h) about 22% wt in the rapid release or immediate release composition and about 78% wt in the extended release composition. 20. The method of claim 17, wherein the MPH salt is MPH hydrochloride. 21. The method of claim 17, wherein the total amount of MPH or salt thereof in the dosage form is about 2.5 mg to about 72 mg, about 20 mg to about 80 mg, or about 18 mg to about 72 mg, about 2.5 mg, about 5 mg, about 7.5 mg, about 9 mg, about 10 mg, about 12.5 mg, about 14 mg, about 15 mg, about 17.5 mg, about 18 mg, about 20 mg, about 25 mg, about 27 mg, about 30 mg, about 35 mg, about 36 mg, about 40 mg, about 45 mg, about 50 mg, about 54 mg, about 60 mg, about 63 mg, about 70 mg, about 72 mg, about 75 mg, about 80 mg, about 81 mg, or about 90 mg. 22. The method of claim 17, wherein a single tablet comprising said total dose is administered daily. 23. The method of claim 17, wherein the condition is selected from the group consisting of attention deficit hyperactivity disorder, narcolepsy, postural orthostatic tachycardia syndrome, lethargy, fatigue, bipolar disorder, lack of attention, opioid induced somnolence, major depressive disorder and obesity.