IP Library Granted Patent US 7,456,254
Granted Patent B2
US 7,456,254 · App. 11/104,877 · Granted Nov 25, 2008

Polymer-based sustained release device

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Quick Facts
Patent No.
US 7,456,254
App. No.
11/104,877
Granted
Nov 25, 2008
Kind
B2
Abstract

This invention relates to compositions for the sustained release of biologically active polypeptides, and methods of forming and using said compositions, for the sustained release of biologically active polypeptides. The sustained release compositions of this invention comprise a biocompatible polymer having dispersed therein, a biologically active polypeptide and a sugar.

Claims (27)

1. A composition for sustained-release of exendin-4, consisting essentially of: a biocompatible polymer having dispersed therein about 3%-5% (w/w) exendin-4 and about 2% (w/w) sucrose, wherein the composition is free from additional ingredients that alter the rate of release of the exendin-4 from the composition.

2. A composition for sustained-release of a polypeptide, consisting of: a biocompatible polymer having dispersed therein about 5% (w/w) exendin-4 and about 2% (w/w) sucrose.

3. A composition for sustained-release of a polypeptide, consisting of: a biocompatible polymer having dispersed therein about 3%-5% (w/w) exendin-4 and about 2% (w/w) sucrose.

4. The composition of claim 1 , wherein the biocompatible polymer is selected from poly(lactides), poly(glycolides), poly(lactide-co-glycolides), poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co-glycolic acid)s and blends and copolymers thereof.

5. The composition of claim 2 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

6. The composition of claim 3 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

7. The composition of claim 1 , wherein the exendin-4 is present at about 5% (w/w) and the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

8. A composition for sustained-release of exendin-4, consisting essentially of: a biocompatible polymer having dispersed therein about 5% (w/w) exendin-4 and about 2% (w/w) sucrose, wherein the composition is free from additional ingredients that alter the rate of release of the exendin-4 from the composition.

9. The composition of claim 8 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1 and a molecular weight in the range of from about 45 to about 64 kDa.

10. The composition of claim 1 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

11. The composition of claim 1 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1 and a molecular weight in the range of from about 45 to about 64 kDa.

12. The composition of claim 2 , wherein the biocompatible polymer is selected from poly(lactides), poly(glycolides), poly(lactide-co-glycolides), poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co-glycolic acid)s and blends and copolymers thereof.

13. The composition of claim 2 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1 and a molecular weight in the range of from about 45 to about 64 kDa.

14. The composition of claim 3 , wherein the biocompatible polymer is selected from poly(lactides), poly(glycolides), poly(lactide-co-glycolides), poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co-glycolic acid)s and blends and copolymers thereof.

15. The composition of claim 3 , wherein the exendin-4 is present at about 5% (w/w) and the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

16. The composition of claim 3 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1 and a molecular weight in the range of from about 45 to about 64 kDa.

17. The composition of claim 8 , wherein the biocompatible polymer is selected from poly(lactides), poly(glycolides), poly(lactide-co-glycolides), poly(lactic acid)s, poly(glycolic acid)s, poly(lactic acid-co-glycolic acid)s and blends and copolymers thereof.

18. The composition of claim 8 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

19. A method of treating a patient having Type 2 diabetes comprising: administering a therapeutically effective amount of a sustained-release composition consisting essentially of a biocompatible polymer having dispersed therein about 3%-5% (w/w) exendin-4 and about 2% (w/w) sucrose, wherein the sustained-release composition is free from additional ingredients that alter the rate of release of the exendin-4 from the sustained-release composition.

20. The method of claim 19 , wherein the exendin-4 is present at about 5% (w/w) and the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

21. The method of claim 19 , wherein the sustained-release composition is administered by injection.

22. The method of claim 19 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

23. The method of claim 20 , wherein the sustained-release composition is administered by injection.

24. A method of treating a patient having Type 2 diabetes comprising: administering a therapeutically effective amount of a sustained-release composition consisting of a biocompatible polymer having dispersed therein about 5% (w/w) exendin-4 and about 2% (w/w) sucrose.

25. The method of claim 24 , wherein the biocompatible polymer is poly(lactide-co-glycolide) with a lactide:glycolide ratio of about 1:1.

26. The method of claim 24 , wherein the sustained-release composition is administered by injection.

27. The method of claim 25 , wherein the sustained-release composition is administered by injection.

Assignments (7)
RELEASE OF PATENT SECURITY AGREEMENT (FIRST LIEN) Recorded Dec 24, 2024
From: MORGAN STANLEY SENIOR FUNDING, INC.
To: ALKERMES, INC.; ALKERMES PHARMA IRELAND LIMITED
Reel/Frame 069771/0548 →
RELEASE BY SECURED PARTY (SECOND LIEN) Recorded Oct 12, 2012
From: MORGAN STANLEY SENIOR FUNDING, INC.
To: ALKERMES, INC.; ALKERMES PHARMA IRELAND LIMITED; ALKERMES CONTROLLED THERAPEUTICS INC.
Reel/Frame 029116/0379 →
CONFIRMATORY ASSIGNMENT Recorded Dec 15, 2011
From: ALKERMES, INC.
To: ALKERMES PHARMA IRELAND LIMITED
Reel/Frame 027396/0409 →
PATENT SECURITY AGREEMENT (FIRST LIEN) Recorded Sep 29, 2011
From: ALKERMES, INC.; ALKERMES PHARMA IRELAND LIMITED; ALKERMES CONTROLLED THERAPEUTICS INC.
To: MORGAN STANLEY SENIOR FUNDING, INC.
Reel/Frame 026994/0186 →
PATENT SECURITY AGREEMENT (SECOND LIEN) Recorded Sep 29, 2011
From: ALKERMES, INC.; ALKERMES PHARMA IRELAND LIMITED; ALKERMES CONTROLLED THERAPEUTICS INC.
To: MORGAN STANLEY SENIOR FUNDING, INC.
Reel/Frame 026994/0245 →
MERGER Recorded Nov 21, 2006
From: ALKERMES CONTROLLED THERAPEUTICS INC. II
To: ALKERMES, INC.
Reel/Frame 018543/0502 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 17, 2005
From: WRIGHT, STEVEN G.; CHRISTENSEN, TROY; YEOH, THEAN Y.; RICKEY, MICHAEL E.; HOTZ, JOYCE M.; KUMAR, RAJESH; COSTANTINO, HENRY R.
To: ALKERMES CONTROLLED THEAPEUTICS, INC. II
Reel/Frame 016644/0608 →