IP Library Patent Application 14484568
Patent Application
App. No. 14/484,568

Stable Formulations of Linaclotide

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Quick Facts
Patent No.
US None
App. No.
14/484,568
Abstract

The present invention relates to stable pharmaceutical compositions comprising linaclotide or pharmaceutically acceptable salts thereof, as well as to various methods and processes for the preparation and use of the compositions.

Claims (26)

1 . A pharmaceutical composition comprising linaclotide, a cation or pharmaceutically acceptable salt thereof and an amine selected from meglumine or a mixture of meglumine and histidine.

2 . The composition of claim 1 , wherein the amine is meglumine.

3 . A pharmaceutical composition comprising linaclotide, a cation or pharmaceutically acceptable salt thereof and histidine, wherein the composition has a molar ratio of cation:histidine of less than 2:1.

4 . The composition of claim 1 or claim 3 , wherein the composition further comprises a polymer.

5 . The composition of claim 4 , wherein the polymer is selected from polyvinyl pyrrolidone (PVP), polyvinyl alcohol (PVA) or a mixture thereof.

6 . A method of treating a gastrointestinal disorder comprising administering to a patient in need thereof, a therapeutically effective amount of the composition of claim 1 or claim 3 .

7 . The method of claim 6 , wherein the gastrointestinal disorder is selected from the group consisting of irritable bowel syndrome, chronic constipation, opioid induced constipation and dyspepsia.

8 . The method of claim 7 , wherein the gastrointestinal disorder is chronic constipation.

9 . The method of claim 7 , wherein the gastrointestinal disorder is constipation-predominant irritable bowel syndrome.

10 . A method of making the composition of claim 1 , comprising combining linaclotide with a cation or pharmaceutically acceptable salt thereof and an amine selected from meglumine or a mixture of meglumine and histidine.

11 . A composition prepared by the method of claim 10 .

12 . A method of making the composition of claim 3 , comprising combining linaclotide with a cation or pharmaceutically acceptable salt thereof and histidine, wherein the composition has a molar ratio of cation:histidine of less than 2:1.

13 . A composition prepared by the method of claim 12 .

14 . A pharmaceutical composition comprising linaclotide, a cation or pharmaceutically acceptable salt thereof and a dipeptide selected from glycine-leucine, leucine-glycine, or a mixture thereof.

15 . The composition of claim 14 , wherein the composition further comprises a polymer.

16 . The composition of claim 15 , wherein the polymer is selected from polyvinyl pyrrolidone (PVP), polyvinyl alcohol (PVA) or a mixture thereof.

17 . A method of treating a gastrointestinal disorder comprising administering to a patient in need thereof, a therapeutically effective amount of the composition of claim 14 .

18 . The method of claim 17 , wherein the gastrointestinal disorder is selected from the group consisting of irritable bowel syndrome, chronic constipation, opioid induced constipation and dyspepsia.

19 . The method of claim 18 , wherein the gastrointestinal disorder is chronic constipation.

20 . The method of claim 18 , wherein the gastrointestinal disorder is constipation-predominant irritable bowel syndrome.

21 . A method of making the composition of claim 14 , comprising combining linaclotide with a cation or pharmaceutically acceptable salt thereof and a dipeptide selected from glycine-leucine, leucine-glycine, or a mixture thereof.

22 . A composition prepared by the method of claim 21 .

23 . The composition of claim 1 , wherein the composition comprises Ca 2+ and an amino acid selected from meglumine or mixture of meglumine and histidine in a molar ratio of Ca 2+ :amino acid between about 1.3:1 and 0.7:1.

24 . The composition of claim 1 , wherein the composition comprises Ca 2+ and an amino acid selected from meglumine or mixture of meglumine and histidine in a molar ratio of Ca 2+ :amino acid between about 1.1:1 and 0.9:1.

25 . The composition of claim 3 , wherein the composition comprises Ca 2+ and histidine in a molar ratio of Ca 2+ :histidine between about 1.3:1 and 0.7:1.

26 . The composition of claim 3 , wherein the composition comprises Ca 2+ and histidine in a molar ratio of Ca 2+ :histidine between about 1.1:1 and 0.9:1.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2015
From: FRETZEN, ANGELIKA; CALI, BRIAN
To: IRONWOOD PHARMACEUTICALS, INC.
Reel/Frame 036496/0150 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 4, 2015
From: MO, YUN; DEDHIYA, MAHENDRA
To: FOREST LABORATORIES HOLDINGS LIMITED
Reel/Frame 036496/0349 →