Methylphenidate extended release chewable tablet
View Patent ↗An oral methylphenidate extended release tablet is described, which can be scored and still retain its extended release profile. The tablet contains a combination of an uncoated methylphenidate-ion exchange resin complex, a barrier coated methylphenidate-ion exchange resin complex-matrix, and an uncomplexed methylphenidate active component. Following administration of a single dose of the extended release methylphenidate chewable tablet, a therapeutically effective amount of methylphenidate is reached in less than about 20 minutes and the composition provides a twelve-hour extended release profile.
1. An extended release racemic methylphenidate chewable tablet, wherein said chewable tablet is a uniform solid dispersion comprising:
a sustained release racemic methylphenidate component comprising a water-insoluble, water-permeable, pH-independent barrier coated, racemic methylphenidate-cation exchange resin complex in an optional polymeric matrix, wherein said barrier coating is present in an amount of about 20% w/w to about 50% w/w % which provides a sustained release profile to the racemic methylphenidate and is over the racemic methylphenidate-cation exchange resin complex-optional matrix, and wherein when present the polymeric matrix comprises the methylphenidate-cation exchange resin complex and a water-insoluble polymer or copolymer or a water-soluble polymer or copolymer; and
at least one immediate release racemic methylphenidate component which provides a release in less than about 30 minutes as determined in an in vitro dissolution assay;
wherein about 50% w/w to about 90% w/w of the racemic methylphenidate active component is provided by the sustained release component based on the total amount of racemic methylphenidate in the tablet;
wherein said chewable tablet is capable of being divided and providing tablet portions which retain a therapeutically effective extended release profile, and a pharmacokinetic profile in which the methylphenidate has at least one of: a geometric mean for area under the curve (AUC) 0-∞ of about 110 ng-hr/mL to about 140 ng-hr/mL or a geometric mean C max of about 10 ng/mL to about 15 ng/mL, under fasted and fed conditions in adults following a single oral administration of a chewable tablet which comprises the equivalent of 40 mg racemic methylphenidate HCl.
2. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the at least one immediate release component releases in about 10 minutes.
3. The extended release racemic methylphenidate chewable tablet according to claim 1 , the sustained release methylphenidate component provides about 60% w/w to about 80% w/w of the methylphenidate in the chewable tablet, based on the total amount of methylphenidate in the tablet.
4. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the at least one immediate release component is a methylphenidate-cation exchange resin complex.
5. The extended release racemic methylphenidate chewable tablet according to claim 4 , wherein the immediate release methylphenidate-cation exchange resin complex comprises about 20% w/w to about 40% w/w of the total racemic methylphenidate in the chewable tablet.
6. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the at least one immediate release component comprises uncomplexed methylphenidate or a pharmaceutically acceptable salt thereof.
7. The extended release racemic methylphenidate chewable tablet according claim 6 , wherein the methylphenidate salt is racemic methylphenidate HCl.
8. The extended release racemic methylphenidate chewable tablet according to claim 6 , wherein the composition comprises immediate release racemic uncomplexed methylphenidate or pharmaceutically acceptable salt in an amount of about 5% w/w to about 35% w/w of the total racemic methylphenidate in the chewable tablet.
9. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the tablet has a hardness in the range of about 8 kp to about 23 kp.
10. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the water insoluble, water-permeable, pH-independent barrier coating has a tensile strength in a range of about 150% to about 400% and is selected from (a) a cured, water-permeable, non-ionic, pH-independent barrier coating comprising polyvinylacetate, a stabilizer, and a plasticizer, applied as an aqueous dispersion; (b) an ionic, pH-independent, acrylic based coating comprising a polymer or copolymer comprising ethyl acrylate and methyl methacrylate applied as an aqueous dispersion; and (c) a solvent-based ethylcellulose coating, optionally with a plasticizer.
11. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the barrier coating over the methylphenidate-cation exchange resin complex-optional matrix of (a) is a cured, water-insoluble, water-permeable, non-ionic, pH-independent barrier coating comprises about 70 to about 90% w/w polyvinylacetate, a stabilizer, and about 2 to about 10% w/w of a plasticizer.
12. The extended release racemic methylphenidate chewable tablet according to claim 11 , wherein the barrier coating layer is about 25% to about 35%, by weight, of the coated racemic methylphenidate-cation exchange resin complex-optional matrix.
13. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the polymeric matrix is present and comprises polyvinylpyrolidone.
14. The extended release chewable racemic methylphenidate tablet according to claim 1 , wherein the polymeric matrix is present and comprises a water-insoluble polymer.
15. The extended release racemic methylphenidate chewable tablet according to claim 14 , wherein the barrier coating over the methylphenidate-cation exchange resin complex-optional matrix of (a) has a pH-independent, acrylic based coating, which said coating comprises a blend of (i) a poly(ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) in a ratio of 1:2:0.1 and (ii) poly(ethyl acrylate-co-methyl methacrylate-co-trimethylammonioethyl methacrylate chloride) in a ratio of 1:2:0.2.
16. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the tablet further comprises a non-functional outer top coating layer.
17. The extended release racemic methylphenidate chewable tablet according to claim 1 which further comprises one or more excipients.
18. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein said tablet is scored.
19. A method for treating a subject having Attention Deficit Hyperactivity Disorder and/or Attention Deficit Disorder with a therapeutically effective amount of racemic methylphenidate, said method comprising orally administering to said subject a single methylphenidate extended release chewable tablet according to claim 1 .
20. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein no more than about 55% of the methylphenidate in the composition is released within one hour as determined in an in vitro dissolution assay.
21. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the tablet comprises more than one immediate release methylphenidate component.
22. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the chewable tablet has a pharmacokinetic profile for racemic methylphenidate comprising a single mean plasma concentration peak.
23. The extended release racemic methylphenidate chewable according to claim 1 , wherein pharmacokinetic profile further comprises the 90% confidence intervals of the geometric test/reference ratios of one or more of AUC0-3 or AUC0-4 of FIG. 1 .
24. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein the methylphenidate plasma concentration, as determined under fasted and fed conditions following a single oral administration of said chewable tablet at a dose equivalent to 40 mg racemic methylphenidate HCl in adults, is equivalent to the plasma concentration curve of FIG. 1 from about 0 to about 8 hours.
25. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein said tablet comprises the equivalent of 40 mg racemic methylphenidate HCl.
26. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein said tablet comprises the equivalent of 20 mg racemic methylphenidate HCl.
27. The extended release racemic methylphenidate chewable tablet according to claim 1 , wherein said tablet comprises the equivalent of 30 mg racemic methylphenidate HCl.