Claims for Patent: 10,610,489

Summary for Patent: 10,610,489

Title:	Pharmaceutical composition, pharmaceutical dosage form, process for their preparation, methods for treating and uses thereof
Abstract:	The present invention relates to pharmaceutical compositions comprising fixed dose combinations of a SGLT-2 inhibitor drug and a partner drug, processes for the preparation thereof, and their use to treat certain diseases.
Inventor(s):	Schneider; Peter (Ulm, DE), Eisenreich; Wolfram (Ulm, DE), Pearnchob; Nantharat (Biberach, DE)
Assignee:	Boehringer Ingelheim International GmbH (Ingelheim am Rhein, DE)
Application Number:	12/894,385
Patent Claims:	1. A pharmaceutical composition comprising a SGLT-2 inhibitor, a partner drug, and one or more pharmaceutical excipients, wherein the SGLT-2 inhibitor is 1-chloro-4-(.beta.-D-glucopyranos-1-yl)-2-[4-((S)-tetrahydrofuran-3-yloxy- )-benzyl]-benzene and wherein the partner drug is metformin hydrochloride, wherein the SGLT-2 inhibitor and metformin hydrochloride are present in a dosage strength of 5 mg/500 mg, 5 mg/850 mg, 5 mg/1,000 mg, 12.5 mg/500 mg, 12.5 mg/850 mg or 12.5 mg/1,000 mg, and wherein said one or more pharmaceutical excipients comprise of one or more fillers comprising microcrystalline cellulose (MCC), D-mannitol, corn starch or pregelatinized starch and a binder comprising copovidone, wherein said pharmaceutical composition is in the dosage form of a tablet, wherein said pharmaceutical composition is an immediate release dosage form, and wherein in a dissolution test after 45 minutes at least 75% by weight of each of the SGLT-2 inhibitor and partner drug is dissolved, wherein the tablet is a mono-layer tablet, wherein the tablet comprises a film-coat, wherein said tablet comprises 3.9-8.3% of said binder by weight of total coated tablet mass. 2. The pharmaceutical composition according to claim 1, wherein the excipients are selected from the group consisting of one or more fillers comprising microcrystalline cellulose (MCC), D-mannitol, corn starch and pregelatinized starch; a binder comprising copovidone; a lubricant comprising magnesium stearate or sodium stearyl fumarate; and a glidant comprising colloidal anhydrous silica. 3. The pharmaceutical composition according to claim 1, further comprising one or more of the following: the filler corn starch, the lubricant magnesium stearate or sodium stearyl fumarate and the glidant colloidal anhydrous silica. 4. The pharmaceutical composition according to claim 1, further comprising one or more of the following: the filler microcrystalline cellulose, the lubricant magnesium stearate or sodium stearyl fumarate and the glidant colloidal anhydrous silica. 5. The pharmaceutical composition according to claim 1, further comprising one or more of the following: the filler microcrystalline cellulose, the lubricant sodium stearyl fumarate and the glidant colloidal anhydrous silica. 6. The pharmaceutical composition according to claim 1, wherein the film-coat comprises a film-coating agent comprising hypromellose; a plasticizer comprising propylene glycol or polyethylene glycol; optionally a glidant comprising talc, and optionally one or more pigments comprising titanium dioxide, iron oxide red and/or iron oxide yellow and/or iron oxide black and mixture thereof. 7. The pharmaceutical composition according to claim 1, wherein the SGLT-2 inhibitor and metformin hydrochloride are present in a dosage strength of 5 mg/500 mg. 8. The pharmaceutical composition according to claim 1, wherein the SGLT-2 inhibitor and metformin hydrochloride are present in a dosage strength of 5 mg/1,000 mg. 9. The pharmaceutical composition according to claim 1, wherein the SGLT-2 inhibitor and metformin hydrochloride are present in a dosage strength of 12.5 mg/500 mg. 10. The pharmaceutical composition according to claim 1, wherein the SGLT-2 inhibitor and metformin hydrochloride are present in a dosage strength of 12.5 mg/1,000 mg. 11. The pharmaceutical composition according to claim 1, further comprising a lubricant. 12. The pharmaceutical composition according to claim 11, wherein said lubricant comprises magnesium stearate or sodium stearyl fumarate. 13. The pharmaceutical composition according to claim 11, wherein said tablet comprises 0.7-1.5% of said lubricant by weight of total coated tablet mass. 14. The pharmaceutical composition according to claim 1, further comprising a glidant. 15. The pharmaceutical composition according to claim 14, wherein said glidant comprises colloidal anhydrous silica. 16. The pharmaceutical composition according to claim 14, wherein said tablet comprises 0.05-0.5% of said glidant by weight of total coated tablet mass. 17. The pharmaceutical composition according to claim 1, further comprising a lubricant and a glidant. 18. The pharmaceutical composition according to claim 17, wherein said lubricant comprises magnesium stearate or sodium stearyl fumarate and said glidant comprises colloidal anhydrous silica. 19. The pharmaceutical composition according to claim 17, wherein said tablet comprises 0.7-1.5% of said lubricant and 0.05-0.5% of said glidant by weight of total coated tablet mass. 20. The pharmaceutical composition according to claim 1, wherein said tablet comprises 2.3-8.0% corn starch, 0-4.4% pregelatinized starch and 0-33% D-mannitol by weight of total coated tablet mass. 21. The pharmaceutical composition according to claim 1, wherein said tablet comprises 0.1-2.11% of said SGLT-2 inhibitor and 47-88% metformin hydrochloride by weight of total coated tablet mass. 22. The pharmaceutical composition according to claim 1, further comprising a disintegrant. 23. The pharmaceutical composition according to claim 22, wherein said disintegrant comprises crospovidone or croscarmellose sodium. 24. The pharmaceutical composition according to claim 1, comprising (% by weight of total coated tablet mass): 0.1-2.11% SGLT-2 inhibitor, 47-88% metformin hydrochloride, 2.3-8.0% corn starch, 0-4.4% pregelatinized starch, 0-33% D-mannitol, and 0.7-1.5% magnesium stearate, said pharmaceutical composition further comprising (% by weight of total coated tablet mass): 0.05-0.5% colloidal anhydrous silica, and 0.00-3.0% disintegrant. 25. The pharmaceutical composition according to claim 24, wherein said disintegrant is crospovidone or croscarmellose sodium. 26. The pharmaceutical composition according to claim 7, comprising 30.130 mg corn starch, and 47.200 mg copovidone, said pharmaceutical composition further comprising 2.950 mg colloidal anhydrous silica and 4.720 mg magnesium stearate. 27. The pharmaceutical composition according to claim 8, comprising 65.260 mg corn starch, and 94.400 mg copovidone, said pharmaceutical composition further comprising 5.900 mg colloidal anhydrous silica and 9.440 mg magnesium stearate. 28. The pharmaceutical composition according to claim 9, comprising 22.630 mg corn starch, and 47.200 mg copovidone, said pharmaceutical composition further comprising 2.950 mg colloidal anhydrous silica and 4.720 mg magnesium stearate. 29. The pharmaceutical composition according to claim 10, comprising 57.760 mg corn starch, and 94.400 mg copovidone, said pharmaceutical composition further comprising 5.900 mg colloidal anhydrous silica and 9.440 mg magnesium stearate.