Orally administered corticosteroid compositions
View Patent ↗The present invention is directed to orally administered corticosteroid compositions. The present invention also provides a method for treating a condition associated with inflammation of the gastrointestinal tract in an individual. The method comprises administering to an individual in need thereof a pharmaceutical composition of the present invention.
1. A method of treating an inflammatory condition of the gastrointestinal tract comprising administering to an individual in need thereof a pharmaceutical composition comprising less than or equal to 20 mg of a topically administrable corticosteroid and at least one excipient,
wherein:
the composition has no significant systemic glucocorticoid or mineralocorticoid activity after oral administration,
the pharmaceutical composition disintegrates within 60 seconds when tested using the USP <701> Disintegration Test, and upon administration the corticosteroid is deposited topically in the upper gastrointestinal tract.
2. The method of claim 1 , wherein said pharmaceutical composition disintegrates within 30 seconds when tested using the USP <701> Disintegration Test.
3. The method of claim 1 , wherein said corticosteroid is selected from the group consisting of budesonide, fluticasone, flunisolide, ciclesonide, mometasone, beclomethasone, and salts, solvates and esters thereof.
4. The method of claim 1 , wherein the pharmaceutical composition is in the form of an orally disintegrating tablet (ODT).
5. The method of claim 4 , wherein the ODT comprises drug particles and rapidly dispersing granules, the drug particles comprise the corticosteroid, the rapidly dispersing granules comprise a disintegrant, the excipient is a sugar alcohol, a saccharide, or a mixture thereof, and the drug particles are disposed over the surface of the rapidly dispersing granules.
6. The method of claim 5 , wherein the drug particles have an average particle size of less than about 400 μm, the rapidly dispersing granules have an average particle size of less than about 300 μm, and the disintegrant and the sugar alcohol, the saccharide, or mixture thereof have an average particle size of less than about 30 μm.
7. The method of claim 5 , wherein the drug particles have an average particle size of less than about 4 μm, the rapidly dispersing granules have an average particle size of less than about 300 μm, and the disintegrant and sugar alcohol, the saccharide, or mixture thereof have an average particle size of less than about 30 μm.
8. The method of claim 5 , wherein the corticosteroid is disposed over the surface of the excipient, the rapidly dispersing granules have an average particle size of less than about 300 μm, and the disintegrant and the sugar alcohol, the saccharide, or mixture thereof have an average particle size of less than about 30 μm.
9. The method of claim 5 , wherein the ODT further comprises microcrystalline cellulose and a pharmaceutically acceptable sweetener, flavorant, and/or colorant, and wherein the excipient is the sugar alcohol.
10. The method of claim 5 , wherein the sugar alcohol is selected from the group consisting of mannitol, xylitol, sorbitol, maltol, maltitol, and combinations thereof.
11. The method of claim 5 , wherein the saccharide is selected from the group consisting of lactose, sucrose, maltose, and combinations thereof.
12. The method of claim 5 , wherein the disintegrant is selected from the group consisting of crospovidone, sodium starch glycolate, crosslinked carboxymethyl cellulose, low-substituted hydroxylpropylcellulose, and combinations thereof.
13. The method of claim 9 , wherein the sugar alcohol is selected from the group consisting of mannitol, xylitol, sorbitol, maltol, maltitol, and combinations thereof.
14. The method of claim 9 , wherein the saccharide is selected from the group consisting of lactose, sucrose, maltose, and combinations thereof.
15. The method of claim 9 , wherein the disintegrant is selected from the group consisting of crospovidone, sodium starch glycolate, crosslinked carboxymethyl cellulose, low-substituted hydroxylpropylcellulose, and combinations thereof.
16. The method of claim 1 , further comprising an adhesive agent.
17. The method of claim 16 , wherein the adhesive agent is selected from the group consisting of sucrose aluminum sulfate complex, chitosan and derivatives thereof, polyvinylpyrrolidone, methylcellulose, sodium carboxymethylcellulose, hydroxypropyl cellulose, cross-linked or uncross-linked polyacrylates, cross-linked polyacrylates, acidic cross-linked or uncross-linked polyacrylates, polyacrylic acid homopolymers or copolymers, aminoalkyl methacrylate copolymers, methacrylic acid/methylmethacrylate copolymer, alkylacrylate/alkylmethacrylate copolymers, ammoniomethacrylate copolymers, carbomer homopolymers or copolymers, hydrophilic polysaccharide gums, maltodextrins, cross-linked alginate gums, polycarboxylated vinyl polymers, pectins, xanthan gums, alginic acid, modified alginic acids, and combinations thereof.
18. The method of claim 1 , further comprising a disintegrant selected from the group consisting of crospovidone, sodium starch glycolate, crosslinked carboxymethyl cellulose, low-substituted hydroxylpropylcellulose, mannitol, xylitol, sorbitol, maltol, maltitol, lactose, sucrose, maltose, and combinations thereof.
19. The method of claim 1 , wherein the excipient is selected from the group consisting of mannitol, xylitol, sorbitol, maltol, maltitol, lactose, sucrose, maltose, cyclodextrin, and combinations thereof.
20. The method of claim 1 , wherein the orally disintegrating solid pharmaceutical composition is substantially free of lubricant.
21. The method of claim 16 , wherein the adhesive agent and the corticosteroid are intimately associated.
22. The method of claim 21 , wherein said corticosteroid is surrounded or encapsulated by the adhesive agent.
23. The method of claim 21 , wherein the corticosteroid is disposed on the surface of said adhesive agent.
24. The method of claim 4 , wherein the ODT comprises a lyophilized matrix, wherein the lyophilized matrix comprises the corticosteroid in combination with at least one excipient.
25. The method of claim 24 , wherein the ODT is in the form of a wafer or film.
26. The method of claim 5 , wherein the ODT is in the form of a wafer or film.
27. The method of claim 1 , further comprising at least one antifungal agent.
28. The method of claim 27 , wherein the antifungal agent is selected from the group consisting of mitotic inhibitor antifungals, pyrimidine analog antifungals, polyene antifungals, benzimidazole antifungals, imidazole antifungals, polyene antifungals, triazole antifungals, thiazole antifungals, allylamine antifungals, echinocandin antifungals, and uncategorized antifungals.
29. The method of claim 28 , wherein the antifungal agent is selected from the group consisting of anidulafungin, caspofungin, clotrimazole, fluconazole, itraconazole, micafungin, nystatin, posaconazole, and voriconazole.
30. The method of claim 1 , further comprising at least one antiviral agent.
31. The method of claim 30 , wherein the antiviral agent is selected from the group consisting of interferons, nucleoside and nucleotide reverse transcriptase inhibitors, non-nucleoside reverse transcriptase inhibitors, protease inhibitors, integrase inhibitors, fusion inhibitors, maturation inhibitors, purine analogs, pyrimidine analogs, and uncategorized antiviral drugs.
32. The method of claim 31 , wherein the antiviral agent is selected from the group consisting of aciclovir, brivudine, docosanol, famciclovir, ganciclocvir, idoxuridine, penciclovir, trifluridine, tromantadine, valaciclovir, and valganciclovir.
33. The method of claim 4 , wherein the orally disintegrating tablet comprises about 0.01 to about 20 mg fluticasone.
34. The method of claim 4 , wherein the orally disintegrating tablet comprises about 0.05-3.0 mg fluticasone.
35. An orally disintegrating solid pharmaceutical composition comprising less than or equal to about 20 mg of a topically administrable corticosteroid and at least one excipient,
wherein:
the solid pharmaceutical composition has no significant systemic glucocorticoid or mineralocorticoid activity after oral administration,
wherein the solid pharmaceutical composition disintegrates within 60 seconds when tested using the USP <701> Disintegration Test, and
upon administration the corticosteroid is deposited topically in the upper gastrointestinal tract.
36. The orally disintegrating solid pharmaceutical composition of claim 35 , wherein said orally disintegrating solid pharmaceutical composition disintegrates within 30 seconds.
37. The orally disintegrating solid pharmaceutical composition of claim 35 , wherein said corticosteroid is selected from the group consisting of budesonide, fluticasone, flunisolide, ciclesonide, mometasone, beclomethasone, and salts, solvates and esters thereof.
38. The orally disintegrating solid pharmaceutical composition of claim 35 , further comprising an adhesive agent.
39. The orally disintegrating solid pharmaceutical composition of claim 35 , wherein the excipient is selected from the group consisting of mannitol, xylitol, sorbitol, maltol, maltitol, lactose, sucrose, maltose, cyclodextrin, and combinations thereof.
40. The orally disintegrating solid pharmaceutical composition of claim 35 , further comprising at least one antifungal agent.
41. The orally disintegrating solid pharmaceutical composition of claim 35 , further comprising at least one antiviral agent.
42. The orally disintegrating solid pharmaceutical composition of claim 35 , wherein the orally disintegrating tablet comprises about 0.01 to about 20 mg fluticasone.