Formulation for Co-Administration of Q-GRFT and Tenofovir
US-2024374681-A1 · Nov 14, 2024 · US
US9763882B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9763882-B2 |
| Application number | US-201214348379-A |
| Country | US |
| Kind code | B2 |
| Filing date | Oct 3, 2012 |
| Priority date | Mar 10, 2011 |
| Publication date | Sep 19, 2017 |
| Grant date | Sep 19, 2017 |
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A composition for use in the treatment of fistula, the composition comprising activated carbon.
Opening claim text (preview).
The invention claimed is: 1. A method for the treatment of fistula, the method comprising administering to a subject in need of such treatment a pharmaceutically effective amount of a composition consisting of particles of activated carbon, wherein the activated carbon is administered rectally as a dry dose, and wherein the activated carbon is driven into the rectum of the subject using a driving fluid. 2. A method according to claim 1 , wherein the activated carbon is of average particle size 0.05 mm to 1 mm. 3. A method according to claim 1 , wherein the activated carbon is of average particle size 0.15 mm to 1 mm. 4. A method for the treatment of fistula, the method comprising administering to a subject in need of such treatment a pharmaceutically effective amount of a composition consisting of particles of activated carbon wherein 85% or more of the activated carbon particles have diameter in the range from 0.089 mm to 0.3 mm, wherein the activated carbon is administered rectally as a dry dose, and wherein the activated carbon is driven into the rectum of the subject using a driving fluid. 5. A method according to claim 4 , wherein 85% or more of the activated carbon particles have diameter in the range from 0.152 mm to 0.297 mm. 6. A method according to claim 1 , wherein the fistula is rectal fistula. 7. A method according to claim 1 , wherein the amount of activated carbon administered is in the range from 450 μg to 10 g. 8. A method according to claim 1 , wherein the activated carbon is granular. 9. A method according to claim 1 , wherein 90% or more of the activated carbon particles have diameter in the range from 0.125 mm to 0.297 mm. 10. A method according to claim 1 , wherein 85% or more of the activated carbon particles have diameter in the range from 0.152 mm to 0.297 mm. 11. A method for the treatment of fistula, the method comprising administering to a subject in need of such treatment a composition consisting of a dry powder of activated carbon which is dust free, wherein the composition is administered rectally as a dry dose, and wherein the activated carbon is driven into the rectum of the subject using a driving fluid. 12. A method for the treatment of fistula, the method comprising administering to a subject in need of such treatment a composition consisting of a dry powder (a dry dose) of activated carbon of particle size 0.001 to 1 mm, wherein the composition is administered rectally, and wherein the activated carbon is driven into the rectum of the subject using a driving fluid. 13. A method according to claim 1 , wherein the activated carbon is of average particle size 0.02 to 1 mm. 14. A method according to claim 1 , wherein the activated carbon is of average particle size 0.15 mm to 0.3 mm. 15. A method according to claim 1 , wherein the fistula is anal fistula. 16. A method according to claim 1 , wherein the activated carbon is ground activated carbon having an irregular particle shape. 17. A method according to claim 1 , wherein the composition is administered using a disposable, rectally-insertable, cannula containing the composition. 18. The method of claim 1 , wherein the driving fluid is a liquid. 19. The method of claim 18 , wherein the driving fluid is water. 20. The method of claim 1 , wherein the driving fluid is a gas. 21. The method of claim 20 , wherein the driving fluid is air. 22. The method of claim 18 , wherein the activated carbon is of particle size 0.15 mm to 1 mm. 23. The method of claim 19 , wherein the activated carbon is of particle size 0.15 mm to 1 mm. 24. The method of claim 18 , wherein the activated carbon is of particle size 0.05 mm to 0.15 mm. 25. The method of claim 19 , wherein the activated carbon is of particle size 0.05 mm to 0.15 mm. 26. The method of claim 20 , wherein the activated carbon is of particle size 0.05 mm to 0.15 mm. 27. The method of claim 21 , wherein the activated carbon is of particle size 0.05 mm to 0.15 mm. 28. The method of claim 1 , wherein the treatment comprises closing the fistula. 29. The method of claim 1 , wherein the treatment comprises healing the fistula, wherein the healing comprises closing the fistula without discharge. 30. The method of claim 1 , wherein the activated carbon is administered twice daily. 31. The method of claim 30 , wherein the activated carbon is administered once in the morning and once in the evening. 32. The method of claim 30 , wherein the treatment comprises closing the fistula within eight weeks of commencing treatment. 33. The method of claim 1 , wherein the driving fluid is maintained separately from the driving fluid until immediately before the activated carbon is administered. 34. A method for the treatment of fistula in a subject in need thereof, the method comprising providing a device containing a formulation that consists of particles of activated carbon as a dry dose, and further contains the driving fluid maintained separately from the activated carbon; inserting the device into the rectum of the subject; and actuating the device to cause the activated carbon to be driven into the rectum of the subject by the driving fluid. 35. The method of claim 34 , wherein the activated carbon is of particle size 0.15 mm to 1 mm and the driving fluid is a liquid; or wherein the activated carbon is of particle size 0.05 mm to 0.15 mm and the driving fluid is a liquid or a gas. 36. The method of claim 35 , wherein the driving fluid is a liquid. 37. The method of claim 36 , wherein the driving fluid is water. 38. The method of claim 35 , wherein the driving fluid is a gas. 39. The method of claim 38 , wherein the driving fluid is air. 40. The method of claim 1 , wherein the treatment is continued for a period of at least 8 weeks. 41. The method of claim 40 , wherein the activated carbon is administered twice daily during the treatment period.
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