IP Library › Granted Patent US 11,753,300
Granted Patent B2
US 11,753,300 · App. 17/469,006 · Granted Sep 12, 2023

Sodium thiosulfate-containing pharmaceutical compositions

Inventors: Craig Sherman (Scottsdale, AZ); Catherine Marie Smith (Grafton, WI); Kevin Robert Wirtz (Belgium, WI); Erich Schulze (Mission Viejo, CA)
Assignee: Hope Medical Enterprises, Inc.
C01B17/64A61K9/0014A61K9/0019A61K31/404A61K31/4418A61K31/519A61K31/573A61K31/60A61K31/727A61K33/00A61K33/04A61K33/14A61K33/22A61K45/06C01P2006/80Y10T436/23
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Quick Facts
Patent No.
US 11,753,300
App. No.
17/469,006
Granted
Sep 12, 2023
Kind
B2
Abstract

Provided herein are pharmaceutically acceptable sodium thiosulfate and pharmaceutical compositions thereof. Also provided herein are methods for determining the total non-purgeable organic carbon in a sodium thiosulfate-containing sample. Further provided herein are methods for producing pharmaceutically acceptable sodium thiosulfate. Still further provided herein are methods of treatment comprising the administration of pharmaceutically acceptable sodium thiosulfate.

Claims (15)

1. A method for treating vascular calcification, calciphylaxis or platinum-induced ototoxicity, comprising administering to a subject having vascular calcification, calciphylaxis or platinum-induced ototoxicity, a pharmaceutical composition comprising a therapeutically effective amount of pharmaceutical grade sodium thiosulfate pentahydrate, wherein the pharmaceutical grade sodium thiosulfate pentahydrate contains no greater than about 8 ppm of non-purgeable organic carbon, contains no greater than about 0.05 ppm of mercury, contains no greater than about 2 ppm of aluminum, contains no greater than about 0.003% by weight of selenium, contains no less than about 98% by weight and no greater than about 102% by weight of sodium thiosulfate on an anhydrous basis measured by ion chromatography, has a water content between 32% and 37% by weight, has a heavy metal content of no greater than about 10 ppm, contains no greater than about 200 ppm of chloride, contains no greater than about 0.001% by weight of sulfide, contains no greater than about 0.002% by weight of iron, contains no greater than about 0.01% by weight of calcium, contains no greater than about 0.005% by weight of potassium, contains no greater than about 0.1% of sulfite, contains no greater than about 0.5% of sulfate, contains no greater than about 3 ppm of arsenic, contains no greater than about 0.001% by weight of lead, has total aerobic count of microbial load of no greater than about 100 CFU/g, has total yeast and mold count of no greater than about 20 CFU/g, contains no greater than about 0.02 EU/mg of bacterial endotoxins, contains no greater than about 0.002% by weight of nitrogen compounds, contains no greater than about 0.005% by weight of insoluble matter, contains no greater than 0.01% by weight of residual anti-caking agent, and contains no greater than ICH Q3C (R3) limits of organic volatile impurities, wherein a 10% aqueous solution of the pharmaceutical grade sodium thiosulfate pentahydrate at 25° C. is colorless and has a pH between about 6.0 and about 8.0, wherein the pharmaceutical grade sodium thiosulfate pentahydrate is odorless crystals, and wherein the pharmaceutical composition further comprises one or more of an isotonic agent, a buffering agent or a pH adjusting agent.

2. The method of claim 1 , wherein vascular calcification is treated.

3. The method of claim 1 , wherein calciphylaxis is treated.

4. The method of claim 1 , wherein platinum-induced ototoxicity is treated.

5. The method of claim 1 , wherein the isotonic agent is potassium chloride, mannitol, sodium chloride, dextran, glucose, glycerin, or dextrose.

6. The method of claim 1 , wherein the buffering agent is phosphate or citrate.

7. The method of claim 1 , wherein the pH adjusting agent is an acid or a base.

8. The method of claim 7 , wherein the acid is boric acid, hydrochloric acid, citric acid or lactic acid.

9. The method of claim 7 , wherein the base is sodium hydroxide.

10. A method for treating atherosclerosis, comprising administering to a subject having atherosclerosis, a pharmaceutical composition comprising a therapeutically effective amount of pharmaceutical grade sodium thiosulfate pentahydrate, wherein the pharmaceutical grade sodium thiosulfate pentahydrate contains no greater than about 8 ppm of non-purgeable organic carbon, contains no greater than about 0.05 ppm of mercury, contains no greater than about 2 ppm of aluminum, contains no greater than about 0.003% by weight of selenium, contains no less than about 98% by weight and no greater than about 102% by weight of sodium thiosulfate on an anhydrous basis measured by ion chromatography, has a water content between 32% and 37% by weight, has a heavy metal content of no greater than about 10 ppm, contains no greater than about 200 ppm of chloride, contains no greater than about 0.001% by weight of sulfide, contains no greater than about 0.002% by weight of iron, contains no greater than about 0.01% by weight of calcium, contains no greater than about 0.005% by weight of potassium, contains no greater than about 0.1% of sulfite, contains no greater than about 0.5% of sulfate, contains no greater than about 3 ppm of arsenic, contains no greater than about 0.001% by weight of lead, has total aerobic count of microbial load of no greater than about 100 CFU/g, has total yeast and mold count of no greater than about 20 CFU/g, contains no greater than about 0.02 EU/mg of bacterial endotoxins, contains no greater than about 0.002% by weight of nitrogen compounds, contains no greater than about 0.005% by weight of insoluble matter, contains no greater than 0.01% by weight of residual anti-caking agent, and contains no greater than ICH Q3C (R3) limits of organic volatile impurities, wherein a 10% aqueous solution of the pharmaceutical grade sodium thiosulfate pentahydrate at 25° C. is colorless and has a pH between about 6.0 and about 8.0, wherein the pharmaceutical grade sodium thiosulfate pentahydrate is odorless crystals, and wherein the pharmaceutical composition further comprises one or more of an isotonic agent, a buffering agent or a pH adjusting agent.

11. The method of claim 10 , wherein the isotonic agent is potassium chloride, mannitol, sodium chloride, dextran, glucose, glycerin, or dextrose.

12. The method of claim 10 , wherein the buffering agent is phosphate or citrate.

13. The method of claim 10 , wherein the pH adjusting agent is an acid or a base.

14. The method of claim 13 , wherein the acid is boric acid, hydrochloric acid, citric acid or lactic acid.

15. The method of claim 13 , wherein the base is sodium hydroxide.

Continuity (12)
Continuation 16905959 · Jun 19, 2020
Continuation 16248026 · Jan 15, 2019
Continuation 16208667 · Dec 4, 2018
Continuation 15916950 · Mar 9, 2018
Continuation 15409659 · Jan 19, 2017
Continuation 15137082 · Apr 25, 2016
Continuation 14310133 · Jun 20, 2014
Continuation 14222766 · Mar 24, 2014
Continuation 13927241 · Jun 26, 2013
Continuation 12831331 · Jul 7, 2010
Provisional Application 61223993 · Jul 8, 2009
Related Publication 20220063999A1 · Mar 3, 2022
Cited By (1)
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