IP Library › Granted Patent US 11,660,276
Granted Patent B2
US 11,660,276 · App. 17/107,724 · Granted May 30, 2023

Compositions and methods for treating chronic inflammation and inflammatory diseases

Inventors: Robin Mark Bannister (Essex, GB); John Brew (Hertfordshire, GB); Wilson Caparros-Wanderley (Buckinghamshire, GB); Gregory Alan Stoloff (London, GB); Suzanne Jane Dilly (Oxfordshire, GB); Gemma Szucs (Oxfordshire, GB); Olga Pleguezuelos Mateo (Bicester, GB)
Assignee: Infirst Healthcare Limited
A61K31/192A61K9/08A61K9/2013A61K31/196A61K31/60A61K47/10A61K47/14A61K47/34A61K47/44A61K31/19A61K31/215A61K31/216A61K31/22A61K31/40Y02A50/30
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Quick Facts
Patent No.
US 11,660,276
App. No.
17/107,724
Granted
May 30, 2023
Kind
B2
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 pharmaceutical composition comprising:

a) a pharmaceutically-acceptable form of a propionic acid derived non-steroidal anti-inflammatory drug (NSAID) in a concentration of about 100 mg/mL to about 1,000 mg/mL;

b) less than about 20% by weight of the composition of a pharmaceutically-acceptable liquid polyethylene glycol (PEG) polymer; and

c) at least 50% by weight of the composition of pharmaceutically-acceptable glycerolipids comprising monoglycerides, diglycerides, and triglycerides;

wherein the pharmaceutical composition is formulated to have a melting point temperature of about 30° C. or higher.

2. The pharmaceutical composition according to claim 1 , wherein the concentration of the propionic acid derived NSAID is about 250 mg/mL to about 750 mg/mL.

3. The pharmaceutical composition according to claim 1 , wherein the concentration of the propionic acid derived NSAID is about 250 mg/mL to about 500 mg/mL.

4. The pharmaceutical composition according to claim 1 , wherein the propionic acid derived NSAID is a pharmaceutically acceptable salt, solvate, or solvate of a salt thereof.

5. The pharmaceutical composition according to claim 1 , wherein the propionic acid derived NSAID comprises 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.

6. The pharmaceutical composition according to claim 1 , wherein the propionic acid derived NSAID is an ester thereof.

7. The pharmaceutical composition according to claim 1 , wherein the liquid PEG polymer is in an amount of less than about 15% by weight of the composition.

8. The pharmaceutical composition according to claim 7 , wherein the liquid PEG polymer is in an amount of about 8% to about 15% by weight of the composition.

9. The pharmaceutical composition according to claim 8 , wherein the liquid PEG polymer is in an amount of about 8% to about 12% by weight of the composition.

10. The pharmaceutical composition according to claim 7 , wherein the liquid PEG polymer is in an amount of about 4% to about 10% by weight of the composition.

11. The pharmaceutical composition according to claim 10 , wherein the liquid PEG polymer is in an amount of about 6% to about 10% by weight of the composition.

12. The pharmaceutical composition according to claim 1 , wherein the liquid PEG polymer is PEG 400.

13. The pharmaceutical composition according to claim 1 , wherein the amount of the pharmaceutically-acceptable glycerolipids is about 50% to about 95% by weight of the composition.

14. The pharmaceutical composition according to claim 1 , wherein the amount of the pharmaceutically-acceptable glycerolipids is at least 60% by weight of the composition.

15. The pharmaceutical composition according to claim 1 , wherein the amount of the triglycerides is at least 30% by weight of the composition.

16. The pharmaceutical composition according to claim 15 , wherein the amount of the triglycerides is at least 35% by weight of the composition.

17. The pharmaceutical composition according to claim 1 , wherein the amount of the monoglycerides is at least 10% by weight of the composition.

18. The pharmaceutical composition according to claim 17 , wherein the amount of the monoglycerides is at least 15% by weight of the composition.

19. The pharmaceutical composition according to claim 1 , wherein the melting point temperature is about 33° C. to about 35° C.

20. The pharmaceutical composition according to claim 1 , wherein the melting point temperature is about 30° C. to about 34° C.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2020
From: BANNISTER, ROBIN M.; BREW, JOHN; CAPARROS-WANDERLEY, WILSON; DILLY, SUZANNE JANE; SZUCS, GEMMA; PLEGUEZUELOS MATEO, OLGA; STOLOFF, GREGORY ALAN
To: BIOCOPEA LIMITED
Reel/Frame 054496/0978 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2020
From: BIOCOPEA LIMITED
To: IMMUNOCOPEA LIMITED
Reel/Frame 054497/0009 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 30, 2020
From: IMMUNOCOPEA LIMITED
To: INFIRST HEALTHCARE LIMITED
Reel/Frame 054497/0042 →
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 16573776 · Sep 17, 2019
Continuation 16012036 · Jun 19, 2018
Continuation 15169619 · May 31, 2016
Continuation 14520150 · Oct 21, 2014
Continuation 13365824 · Feb 3, 2012
Continuation In Part PCTGB2011052115 · Oct 31, 2011
Related Publication 20210077441A1 · Mar 18, 2021
Cited By (1)
US 12,533,332