Granted Patent B2

US 12,285,521 · App. 17/811,970 · Granted Apr 29, 2025

Inventors: Scott Boyer (Uppsala, SE); Fredrik Hübinette (Uppsala, SE); Leif Ingemarsson (Uppsala, SE); Susan Suchdev (Uppsala, SE)

Assignee: Klaria Pharma Holding AB

A61K9/006A61K31/4045A61K31/734A61K47/02A61K47/10

Abstract

Claims (40)

1. An oral transmucosal film suitable for administration to an oral cavity, comprising:

(i) an alginate salt of a monovalent cation or a mixture of alginate salts containing at least one alginate salt of a monovalent cation;

(ii) sumatriptan or a pharmaceutically acceptable salt thereof; and

(iii) citric acid, or a pharmaceutically acceptable salt of citrate, or both citric acid and a pharmaceutically acceptable salt of citrate;

wherein the alginate salt of a monovalent cation (a) comprises from 25% to 35% by weight of β-D-mannuronate and/or from 65% to 75% by weight of α-L-guluronate, and (b) has a mean molecular weight of from 30,000 g/mol to 90,000 g/mol.

2. The film according to claim 1 , wherein the alginate salt of a monovalent cation is a sodium alginate, a potassium alginate or an ammonium alginate.

3. The film according to claim 2 , wherein the alginate salt of a monovalent cation is a sodium alginate.

4. The film according to claim 1 , wherein:

the film comprises from 25% to 99% by weight of the alginate salt of a monovalent cation or the mixture of alginate salts containing at least one alginate salt of a monovalent cation, from 0% to 20% by weight of water, and from 0.001% to 75% by weight of sumatriptan or the pharmaceutically acceptable salt thereof; or

the film comprises from 30% to 86% by weight of the alginate salt of a monovalent cation or the mixture of alginate salts containing at least one alginate salt of a monovalent cation, from 5% to 15% by weight of water, and from 4% to 40% by weight of sumatriptan.

5. A method of treating migraine with or without aura, cluster headache, or trigeminal neuralgia in a human patient, wherein said method comprises administration of at least one film according to claim 1 to said human patient.

6. The method according to claim 5 , wherein the film is administered to the oral cavity of the human patient.

7. A method of manufacturing a film according to claim 1 , said method, comprising:

(a) mixing sumatriptan or a pharmaceutically acceptable salt thereof and citric acid, or a pharmaceutically acceptable salt of citrate, or both citric acid and a pharmaceutically acceptable salt of citrate, in water;

(b) adjusting the pH of the solution to the desired level by addition of an appropriate acid or base, typically a diluted aqueous acid or alkali;

(c) optionally, adding further water and/or one or more plasticizers under further mixing;

(d) adding the alginate salt of monovalent cation under suitable conditions to result in the formation of a viscous cast;

(e) pouring the cast onto a surface and spreading the cast out to the desired thickness;

(f) drying the cast layer until the residual water content of the film is from 5 to 15% by weight and a solid film is formed; and

(g) optionally, cutting the solid film into pieces of the desired size, further optionally placing these pieces into pouches, sealing the pouches and further optionally, labelling them.

8. The method according to claim 5 , wherein the human patient i) suffers from nausea and/or dysphagia and/or (ii) is additionally receiving treatment for one or more types of cancer.

9. The method according to claim 7 , wherein in (b), the pH of the solution is adjusted to from 3.25 to 10.0.

10. The film according to claim 1 , wherein the pharmaceutically acceptable salt of sumatriptan is succinate, tartrate, citrate, fumarate, malonate, maleate, adipate, di-mesylate, sulfate, benzenesulfonate, hydrochloride, or phosphate salts.

11. The film according to claim 1 , wherein the pharmaceutically acceptable salt of citrate is a sodium salt, a potassium salt or an ammonium salt.

12. The film according to claim 1 , wherein the film comprises from 0.1% to 10% by weight of the pharmaceutically acceptable salt of citrate.

13. The film according to claim 1 , wherein the film comprises a buffering component which is a pharmaceutically acceptable salt of citrate and an acidifying agent which is citric acid.

14. The film according to claim 1 , wherein the concentration of citric acid in the film is from 1 mM to 40 mM, or from 5 mM to 20 mM.

15. The film according to claim 1 , wherein the film further comprises a plasticizer selected from polyethylene glycol, glycerol, sorbitol, xylitol or a combination thereof.

16. The film according to claim 15 , wherein the film comprises from 5% to 40% by weight of glycerol and from 5% to 40% by weight of sorbitol.

17. An oral transmucosal film suitable for administration to an oral cavity, comprising:

(i) an alginate salt of a monovalent cation or a mixture of alginate salts containing at least one alginate salt of a monovalent cation; and

(ii) a citrate salt of sumatriptan;

wherein the alginate salt of a monovalent cation (a) comprises from 25% to 35% by weight of β-D-mannuronate and/or from 65% to 75% by weight of α-L-guluronate, and (b) has a mean molecular weight of from 30,000 g/mol to 90,000 g/mol.

18. The film according to claim 17 , wherein the alginate salt of a monovalent cation is a sodium alginate.

19. The film according to claim 17 , wherein:

the film comprises from 25% to 99% by weight of the alginate salt of a monovalent cation or the mixture of alginate salts containing at least one alginate salt of a monovalent cation, from 0% to 20% by weight of water, from 0.001% to 75% by weight of sumatriptan citrate, from 0% to 40% by weight of glycerol and from 0% to 40% by weight of sorbitol; or

the film comprises from 30% to 86% by weight of the alginate salt of a monovalent cation or the mixture of alginate salts containing at least one alginate salt of a monovalent cation, from 5% to 15% by weight of water, from 4% to 40% by weight of sumatriptan citrate, from 5% to 40% by weight of glycerol and from 5% to 40% by weight of sorbitol.

20. A method of treating migraine with or without aura, cluster headache, or trigeminal neuralgia in a human patient, wherein said method comprises administration of at least one film according to claim 17 to a human patient,

optionally wherein the film is administered to the oral cavity of the human patient;

further optionally wherein the human patient (i) suffers from nausea and/or dysphagia and/or (ii) is additionally receiving treatment for one or more types of cancer.

Assignments (1)

Priority Claims (1)

Continuity (3)

References Cited (260)