IP Library › Granted Patent US 11,202,831
Granted Patent B2
US 11,202,831 · App. 16/882,666 · Granted Dec 21, 2021

Solid solution compositions and use in cardiovascular disease

Inventors: Robin M. Bannister (Essex, GB); John Brew (Hertfordshire, GB); Richard R. Reiley, III (London, GB); Wilson Caparros Wanderley (Buckinghamshire, GB)
Assignee: Infirst Healthcare Limited
A61K47/14A61K9/08A61K9/145A61K31/121A61K31/137A61K31/167A61K31/192A61K31/196A61K31/222A61K31/357A61K31/366A61K31/4178A61K31/4184A61K31/522A61K31/60A61K31/616A61K47/10A61K47/22A61K47/44A61K9/2013Y02A50/30
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Quick Facts
Patent No.
US 11,202,831
App. No.
16/882,666
Filed
May 25, 2020
Granted
Dec 21, 2021
Kind
B2
Art Unit
1613
USPC
424/400
Abstract

The present specification discloses pharmaceutical compositions, methods of preparing such pharmaceutical compositions, and methods and uses of treating a chronic inflammation and/or an inflammatory disease in an individual using such pharmaceutical compositions.

Claims (24)

1. A solid solution pharmaceutical composition comprising:

a) a peroxisome proliferator-activator receptor gamma (PPAR-γ) agonist;

b) one or more pharmaceutically-acceptable hard fats comprising one or more glycerolipids, the one or more pharmaceutically-acceptable hard fats in an amount of at least 30% by weight of the pharmaceutical composition;

c) one or more pharmaceutically-acceptable liquid lipids comprising one or more partially hydrolyzed fats, the one or more pharmaceutically-acceptable liquid lipids in an amount of less than 45% by weight of the pharmaceutical composition, and

wherein the solid solution pharmaceutical composition is formulated to be a solid at a temperature of about 15° C. or lower and has a melting point of 30° C. or higher.

2. The solid solution pharmaceutical composition according to claim 1 , wherein the PPAR-γ agonist is about 10% to about 40% by weight of the pharmaceutical composition.

3. The solid solution pharmaceutical composition according to claim 2 , wherein the PPAR-γ agonist is about 15% to about 35% by weight of the pharmaceutical composition.

4. The solid solution pharmaceutical composition according to claim 3 , wherein the PPAR-γ agonist is in an amount from about 20% to about 30% by weight of the pharmaceutical composition.

5. The solid solution pharmaceutical composition according to claim 1 , wherein the PPAR-γ agonist comprises a non-steroidal anti-inflammatory drug (NSAID), a fibrate, a thiazolidinedione, or a combination thereof.

6. The solid solution pharmaceutical composition according to claim 5 , wherein the NSAID comprises a non-selective cyclooxygenase inhibitor, a selective cyclooxygenase 1 inhibitor, a selective cyclooxygenase 2 inhibitor or any combination thereof.

7. The solid solution pharmaceutical composition according to claim 5 , wherein the NSAID comprises a salicylate derivative NSAID, a p-amino phenol derivative NSAID, a propionic acid derivative NSAID, an acetic acid derivative NSAID, an enolic acid derivative NSAID, a fenamic acid derivative NSAID or a combination thereof.

8. The solid solution pharmaceutical composition according to claim 7 , wherein the propionic acid derivative NSAID comprises a pharmaceutically-acceptable form of an Alminoprofen, a Benoxaprofen, a Dexketoprofen, a Fenoprofen, a Flurbiprofen, an Ibuprofen, an Indoprofen, a Ketoprofen, a Loxoprofen, a Naproxen, an Oxaprozin, a Pranoprofen, or a Suprofen.

9. The solid solution pharmaceutical composition a according to claim 5 , wherein the fibrate comprises Bezafibrate, Ciprofibrate, Clofibrate, Gemfibrozil, Fenofibrate, or a combination thereof.

10. The solid solution pharmaceutical composition according to claim 1 , wherein the amount of the one or more pharmaceutically-acceptable hard fats is at least 35% by weight of the pharmaceutical composition.

11. The solid solution pharmaceutical composition according to claim 1 , wherein the amount of the one or more pharmaceutically-acceptable hard fats is about 20% to about 50% by weight of the pharmaceutical composition.

12. The solid solution pharmaceutical composition according to claim 11 , wherein the amount of the one or more pharmaceutically-acceptable hard fats is about 30% to about 50% by weight of the pharmaceutical composition.

13. The solid solution pharmaceutical composition according to claim 12 , wherein the amount of the one or more pharmaceutically-acceptable hard fats is about 35% to about 45% by weight of the pharmaceutical composition.

14. The solid solution pharmaceutical composition according to claim 1 , wherein the one or more pharmaceutically-acceptable hard fats have a melting point of about 40° C. to about 46° C.

15. The solid solution pharmaceutical composition according to claim 14 , wherein the one or more pharmaceutically-acceptable hard fats comprises a mixture of saturated C 10 -C 18 triglycerides having a melting point of between 41° C. to 45° C.

16. The solid solution pharmaceutical composition according to claim 1 , wherein the amount of the one or more pharmaceutically-acceptable liquid lipids is less than 40% by weight of the pharmaceutical composition.

17. The solid solution pharmaceutical composition according to claim 1 , wherein the amount of the one or more pharmaceutically-acceptable liquid lipids is about 10% to about 30% by weight of the pharmaceutical composition.

18. The solid solution pharmaceutical composition according to claim 17 , wherein the amount of the one or more pharmaceutically-acceptable liquid lipids is about 15% to about 25% by weight of the pharmaceutical composition.

19. The solid solution pharmaceutical composition according to claim 1 , wherein the mixture of one or more partially hydrolyzed fats comprises a mixture of one or more monoglycerides, one or more diglycerides, and one or more triglycerides.

20. The solid solution pharmaceutical composition according to claim 19 , wherein the one or more monoglycerides comprise glyceryl monolinoleate.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2020
From: BANNISTER, ROBIN M.; BREW, JOHN; CAPARROS WANDERLEY, WILSON
To: BIOCOPEA LIMITED
Reel/Frame 052743/0233 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2020
From: REILEY, RICHARD R.
To: BIOCOPEA LIMITED
Reel/Frame 052743/0240 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2020
From: BIOCOPEA LIMITED
To: IMMUNOCOPEA LIMITED
Reel/Frame 052743/0243 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 25, 2020
From: IMMUNOCOPEA LIMITED
To: INFIRST HEALTHCARE LIMITED
Reel/Frame 052743/0258 →
Priority Claims (5)
GB 1018289 · Oct 29, 2010 · national
GB 1101937 · Feb 4, 2011 · national
GB 1113728 · Aug 10, 2011 · national
GB 1113729 · Aug 10, 2011 · national
GB 1113730 · Aug 10, 2011 · national
Continuity (7)
Continuation 14155147 · Jan 14, 2014
Continuation In Part 13365824 · Feb 3, 2012
Continuation In Part PCTGB2011052115 · Oct 31, 2011
Continuation In Part 13365828 · Feb 3, 2012
Provisional Application 61752309 · Feb 4, 2013
Provisional Application 61752356 · Jan 14, 2013
Related Publication 20200297850A1 · Sep 24, 2020
Cited By (2)
US 12,533,332 US 12,685,709