Claims for Patent: 6,589,556

Summary for Patent: 6,589,556

Title:	Rapid-melt semi-solid compositions, methods of making same and methods of using same
Abstract:	A novel rapid-melt, semi-solid molded composition, including methods of making the same, and methods of using the same for the delivery of prophylactic and therapeutic active materials to a mammal wherein the prophylactic or therapeutic active is a psychotropic, a gastrointestinal therapeutic or a migraine therapeutic.
Inventor(s):	Cherukuri; Subraman Rao (Vienna, VA)
Assignee:	Capricorn Pharma, Inc. (Frederick, MD)
Application Number:	09/858,885
Patent Litigation and PTAB cases:	See patent lawsuits and PTAB cases for patent 6,589,556
Patent Claims:	1. A rapid melt, semi-solid molded composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; and a therapeutically effective amount of a drug, wherein said drug is selected from the group consisting of psychotropics, gastrointestinal therapeutics, cardiovascular therapeutics, migraine therapeutics, inflammation therapeutics, benign prostatic hypertrophy therapeutics, fungal therapeutics, allergic rhinitis therapeutics, anticonvulsants, and viral therapeutics. 2. The composition of claim 1, wherein the said drug is a psychotropic. 3. The composition of claim 2, wherein said psychotropic is a anti-anxiety therapeutic. 4. The composition of claim 2, wherein said psychotropic is an insomnia therapeutic. 5. The composition of claim 2, wherein said psychotropic is an antidepressant. 6. The composition of claim 5, wherein said antidepressant is selected from the group consisting of Fluoxetine HCl, Paroxetine HCl, Sertraline HCl, and Venlafaxine HCl, Amitriptyline, Nortriptyline, Imipramine, Desipramine, Doxepin, Trimipramine, Clomipramine, Protriptyline, Amoxapine, Maprotiline, Phenelzine, Tranylcypromine, Fluvoxamine, Venlafaxine, Trazodone, Nefazodone, Mirtazapine, Bupropion, or mixtures thereof. 7. The composition of claim 6, wherein said drug is Fluoxetine HCl. 8. The composition of claim 1, wherein said drug is a gastrointestinal therapeutic. 9. The composition of claim 8, wherein said gastrointestinal therapeutic is a ulcer therapeutic. 10. The composition of claim 9, wherein said ulcer therapeutic is selected from the group consisting of Omeprazole, Lansoprazole, Ranitidine HCl, Famotidine, Nizatidine, Teprenone, Cimetidine, Rabeprazole sodium, Sulpiride, or mixtures thereof. 11. The composition of claim 10, wherein said ulcer therapeutic is Omeprazole. 12. The composition of claim 8, wherein said gastrointestinal therapeutic is a anti-emetic. 13. The composition of claim 12, wherein said anti-emetic is selected from the group consisting of Ondansetron HCl, Granisetron HCl, Tropisetron, Dolasetron mesylate, Cisapride, Sulfasalazine, Balsalazide, Infliximab, or mixtures thereof. 14. The composition of claim 8, wherein said gastrointestinal therapeutic is a anti-diarrheal therapeutic. 15. The composition of claim 14, wherein said anti-diarrheal therapeutic is selected from the group consisting of Loperamide HCl, diphenoxylate, codeine phosphate, camphorated opium tincture, or mixtures thereof. 16. The composition of claim 15, wherein said anti-diarrheal therapeutic is Loperamide HCl. 17. The composition of claim 1, wherein said drug is a migraine therapeutic. 18. The composition of claim 17, wherein said migraine therapeutic is selected from the group consisting of sumatriptan succinate, amitripyline, methysergide, propranolol, valproate, verapamil, dihydroergotamine, ergotamine, metoclopramide, naratriptan, prochlorperazine, rizatriptan benzoate, zolmitriptan, eletriptan, acetaminophen, aspirin, NSAID's, opioids, or mixtures thereof. 19. The composition of claim 18, wherein said migraine therapeutic is sumatriptan succinate. 20. A method of preparing a rapid-melt, semi-solid molded composition comprising the steps of: a) melting at least one binder in an amount from about 0.01% to about 70% by weight with a salivating agent in an amount from about 0.05% to about 15% by weight, to form a mixture; b) mixing a therapeutically effective amount of a drug with said mixture to form an active mixture; said drug selected from the group consisting of psychotropics, gastrointestinal therapeutics, cardiovascular therapeutics, migraine therapeutics, inflammation therapeutics, benign prostatic hypertrophy therapeutics, fungal therapeutics, allergic rhinitis therapeutics, anticonvulsants, and viral therapeutics. c) mixing a diluent/bulking material with said active mixture to form a final mixture; and d) molding said final mixture into said rapid-melt, semi-solid molded composition. 21. The method of claim 20, wherein said drug is a psychotropic. 22. The method of claim 21, wherein said psychotropic is selected from the group consisting of Fluoxetine HCl, Paroxetine HCl, Sertraline HCl, and Venlafaxine, Amitriptyline, Nortriptyline, Imipramine, Desipramine, Doxepin, Trimipramine, Clomipramine, Protriptyline, Amoxapine, Maprotiline, Phenelzine, Tranylcypromine, Fluvoxamine, Venlafaxine, Trazodone, Nefazodone, Mirtazapine, Bupropion, or mixtures thereof. 23. The method of claim 22, wherein said psychotropic is Fluoxetine HCl. 24. The method of claim 20, wherein said drug is a gastrointestinal therapeutic. 25. The method of claim 24, wherein said gastrointestinal therapeutic is a ulcer therapeutic. 26. The method of claim 25, wherein said ulcer therapeutic is selected from the group consisting of Omeprazole, Lansoprazole, Ranitidine HCL, Famotidine, Nizatidine, Teprenone, Cimetidine, Rabeprazole sodium, Sulpiride, or mixtures thereof. 27. The method of claim 26, wherein said ulcer therapeutic is Omeprazole. 28. The method of claim 24, wherein said gastrointestinal therapeutic is a anti-emetic. 29. The method of claim 28, wherein said anti-emetic is selected from the group consisting of Ondansetron HCl, Granisetron HCl, Tropisetron, Dolasetron mesylate, Cisapride, Sulfasalazine, Balsalazide, Infliximab, or mixtures thereof. 30. The method of claim 24, wherein said gastrointestinal therapeutic is a anti-diarrheal therapeutic. 31. The method of claim 30, wherein said anti-diarrheal therapeutic is selected from the group consisting of Loperamide HCl, diphenoxylate, codeine phosphate, camphorated opium tincture, or mixtures thereof. 32. The method of claim 31, wherein said anti-diarrheal therapeutic is Loperamide HCl. 33. The method of claim 20, wherein said drug is a migraine therapeutic. 34. The method of claim 33, wherein said migraine therapeutic is selected from the group consisting of sumatriptan succinate, amitripyline, methysergide, propranolol, valproate, verapamil, dihydroergotamine, ergotamine, metoclopramide, naratriptan, prochlorperazine, rizatriptan benzoate, zolmitriptan, eletriptan, acetaminophen, aspirin, NSAID's, opioids, or mixtures thereof. 35. The method of claim 34, wherein said migraine therapeutic is sumatriptan succinate. 36. A method for treating depression, anxiety or insomnia comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an anti-depressant, anti-anxiety therapeutic or an insomnia therapeutic and wherein said composition is prepared in the absence of free water. 37. A method for treating diarrhea and nausea comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an gastrointestinal therapeutic, a anti-emetic or a anti-diarrheal therapeutic and wherein said composition is prepared in the absence of free water. 38. A method for treating migraines comprising the step of administering to a patient in need thereof a pharmaceutical composition comprising: at least one binder in an amount from about 0.01% to about 70% by weight; a salivating agent in an amount from about 0.05% to about 15% by weight; a diluent/bulking material in an amount from about 10% to about 90% by weight; a therapeutically effective amount of an migraine therapeutic and wherein said composition is prepared in the absence of free water.

Details for Patent 6,589,556

Applicant	Tradename	Biologic Ingredient	Dosage Form	BLA	Approval Date	Patent No.	Expiredate
Janssen Biotech, Inc.	REMICADE	infliximab	For Injection	103772	08/24/1998		2020-07-05