Claims for Patent: 11,234,938

Summary for Patent: 11,234,938

Title:	Pharmaceutical composition, comprising phosphate binder particles
Abstract:	The present invention relates to pharmaceutical composition, comprising certain phosphate binder particles having a certain particle size distribution, a process for the manufacture of the pharmaceutical composition and the use of sucroferric oxyhydroxide having a certain particle size distribution for the manufacture of a pharmaceutical composition.
Inventor(s):	Chofflon; Laurent (Zurich, CH), Philipp; Erik (Arbon, CH)
Assignee:	Vifor Fresenius Medical Care Renal Pharma Ltd. (St. Gallen, CH)
Application Number:	16/820,190
Patent Claims:	1. A pharmaceutical composition for oral administration comprising sucroferric oxyhydroxide; wherein the pharmaceutical composition is in the form of a chewable tablet; wherein the chewable tablet has a disintegration time of between 5 minutes and 18 minutes as measured according to the European Pharmacopoeia 04/2011:20901; wherein the hardness of the chewable tablet is between 100 N to 200 N as measured according to the European Pharmacopoeia 01/2008:20908; wherein the weight of the chewable tablet is between 2000 mg and 3000 mg; wherein more than 65% of the weight of the chewable tablet (by weight on a dry weight basis) is sucroferric oxyhydroxide; and wherein the chewable tablet is prepared using sucroferric oxyhydroxide particles, wherein at least 80% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 4 .mu.m to 200 .mu.m and the d50 particle size distribution by volume of the sucroferric oxyhydroxide particles is in the range of 40 .mu.m to 80 .mu.m. 2. The pharmaceutical composition according to claim 1, wherein at least 80% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 5 .mu.m to 160 .mu.m. 3. The pharmaceutical composition according to claim 1, wherein at least 90% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 4 .mu.m to 200 .mu.m. 4. The pharmaceutical composition according to claim 1, wherein the friability of the chewable tablet is between 0% to 7% as measured according to the European Pharmacopoeia 01/2010:20907. 5. The pharmaceutical composition according to claim 1, wherein the chewable tablet is formed by direct compression. 6. A pharmaceutical composition for oral administration comprising about 2500 mg of sucroferric oxyhydroxide; wherein the pharmaceutical composition is in the form of a chewable tablet; wherein the chewable tablet has a disintegration time of between 5 minutes and 18 minutes as measured according to the European Pharmacopoeia 04/2011:20901; wherein the hardness of the chewable tablet is between 100 N to 200 N as measured according to the European Pharmacopoeia 01/2008:20908; wherein more than 65% of the weight of the chewable tablet (by weight on a dry weight basis) is sucroferric oxyhydroxide; and wherein the chewable tablet is prepared using sucroferric oxyhydroxide particles, wherein at least 80% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 4 .mu.m to 200 .mu.m and the d50 particle size distribution by volume of the sucroferric oxyhydroxide particles is in the range of 40 .mu.m to 80 .mu.m. 7. The pharmaceutical composition according to claim 6, wherein at least 80% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 5 .mu.m to 160 .mu.m. 8. The pharmaceutical composition according to claim 6, wherein the chewable tablet is a compressed tablet. 9. The pharmaceutical composition according to claim 6, wherein the chewable tablet is formed by direct compression. 10. The pharmaceutical composition according to claim 6, wherein the friability of the tablet is between 0% to 7% as measured according to the European Pharmacopoeia 01/2010:20907. 11. A pharmaceutical composition for oral administration comprising sucroferric oxyhydroxide; wherein the pharmaceutical composition is in the form of a chewable tablet; wherein the weight of the chewable tablet is between 2000 mg and 3000 mg; wherein the chewable tablet has a disintegration time of between 5 minutes and 18 minutes as measured according to the European Pharmacopoeia 04/2011:20901; wherein the hardness of the chewable tablet is between 100 N to 200 N as measured according to the European Pharmacopoeia 01/2008:20908; wherein more than 80% of the weight of the chewable tablet (by weight on a dry weight basis) is sucroferric oxyhydroxide; and wherein the chewable tablet is prepared using sucroferric oxyhydroxide particles, wherein at least 80% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 4 .mu.m to 200 .mu.m and the d50 particle size distribution by volume of the sucroferric oxyhydroxide particles is in the range of 40 .mu.m to 80 .mu.m. 12. The pharmaceutical composition according to claim 11, wherein at least 80% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 5 .mu.m to 160 .mu.m. 13. The pharmaceutical composition according to claim 11, wherein at least 90% by volume of the sucroferric oxyhydroxide particles have a particle size in the range of 5 .mu.m to 160 .mu.m. 14. The pharmaceutical composition according to claim 11, wherein the chewable tablet is a compressed tablet. 15. The pharmaceutical composition according to claim 11, wherein the chewable tablet is formed by direct compression. 16. The pharmaceutical composition according to claim 11, wherein the friability of the chewable tablet is between 0% to 7% as measured according to the European Pharmacopoeia 01/2010:20907.