IP Library › Granted Patent US 10,695,431
Granted Patent B2
US 10,695,431 · App. 14/155,147 · Granted Jun 30, 2020

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
A61K47/14A61K9/08A61K9/145A61K31/121A61K31/137A61K31/167A61K31/192A61K31/196A61K31/222A61K31/357A61K31/366A61K31/4178A61K31/4184A61K31/522A61K31/60A61K31/616A61K47/10A61K47/22A61K47/44A61K9/2013Y02A50/411
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Quick Facts
Patent No.
US 10,695,431
App. No.
14/155,147
Filed
Jan 14, 2014
Granted
Jun 30, 2020
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 (33)

1. A solid solution pharmaceutical composition comprising:

a) one or more statins in an amount of about 1% to 30% by weight of the pharmaceutical composition;

b) one or more pharmaceutically-acceptable hydrophobic hard fats in an amount of about 30% to about 75% by weight of the pharmaceutical composition, the one or more pharmaceutically-acceptable hydrophobic hard fats consisting of a mixture of saturated C 10 -C 18 triglycerides having a melting point range of 41° C. to 45° C.; and

c) one or more pharmaceutically-acceptable hydrophobic liquid fats in an amount of about 8% to about 40% by weight of the pharmaceutical composition, the one or more pharmaceutically-acceptable liquid fats being liquid at 20° C. and comprising monoglycerides;

wherein the solid solution pharmaceutical composition does not comprise a pharmaceutically-acceptable hydrophilic solvent;

wherein the solid solution pharmaceutical composition is not a multi-phasic 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 one or more statins is in an amount of about 1% to about 20% by weight of the pharmaceutical composition.

3. The solid solution pharmaceutical composition according to claim 1 , wherein the one or more pharmaceutically-acceptable hard fat is in an amount of at least 50% by weight of the pharmaceutical composition.

4. The solid solution pharmaceutical composition according to claim 1 , wherein the monoglycerides are in an amount of less than 35% by weight of the pharmaceutical composition.

5. The solid solution pharmaceutical composition according to claim 1 , wherein the one or more statins includes Atorvastatin, Fluvastatin, Lovastatin, Pitavastatin, Pravastatin, Rosuvastatin, and Simvastatin.

6. The solid solution pharmaceutical composition according to claim 1 , wherein the monoglycerides comprise glycerol monomyristoleate, glycerol monopalmitoleate, glycerol monosapienate, glycerol monooleate, glycerol monoelaidate, glycerol monovaccenate, glycerol monolinoleate, glycerol monolinoelaidate, glycerol monolinolenate, glycerol monostearidonate, glycerol monoeicosenoate, glycerol monomeadate, glycerol monoarachidonate, glycerol monoeicosapentaenoate, glycerol monoerucate, glycerol monodocosahexaenoate, or glycerol mononervonate.

7. The solid solution pharmaceutical composition according to claim 6 , wherein the one or more pharmaceutically-acceptable monoglycerides comprises glycerol monolinoleate.

8. The solid solution pharmaceutical composition according to claim 2 , wherein the one or more statins has is about 1% to about 15% by weight of the pharmaceutical composition.

9. The solid solution pharmaceutical composition according to claim 3 , wherein the one or more pharmaceutically-acceptable hard fat is at least 55% by weight of the pharmaceutical composition.

10. The solid solution pharmaceutical composition according to claim 9 , wherein the one or more pharmaceutically-acceptable hard fat is at least 60% by weight of the pharmaceutical composition.

11. The solid solution pharmaceutical composition according to claim 1 , wherein the one or more pharmaceutically-acceptable hard fat consisting of consists of a mixture of saturated C 10 -C 18 triglycerides having a melting point range of about 43° C.

12. A solid solution pharmaceutical composition consisting essentially of:

a) one or more statins in an amount of about 1% to 30% by weight of the pharmaceutical composition;

b) one or more pharmaceutically-acceptable hydrophobic hard fats in an amount of about 30% to about 75% by weight of the pharmaceutical composition, the one or more pharmaceutically-acceptable hydrophobic hard fats consisting of a mixture of saturated C 10 -C 18 triglycerides having a melting point range of 41° C. to 45° C.; and

c) one or more pharmaceutically-acceptable hydrophobic monoglycerides in an amount of about 8% to about 40% by weight of the pharmaceutical composition, the one or more pharmaceutically-acceptable monoglycerides being liquid at 20° C.;

wherein the solid solution pharmaceutical composition does not comprise a pharmaceutically-acceptable hydrophilic solvent;

wherein the solid solution pharmaceutical composition is not a multi-phasic 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.

13. The solid solution pharmaceutical composition according to claim 12 , wherein the one or more statins is in an amount of about 1% to 20% by weight of the pharmaceutical composition, the one or more pharmaceutically-acceptable hard fats is in an amount of at least 50% by weight of the pharmaceutical composition and the one or more pharmaceutically-acceptable monoglycerides is in an amount of less than 35% by weight of the pharmaceutical composition.

14. A solid solution pharmaceutical composition consisting essentially of:

a) a statin in an amount of about 1% to 30% by weight of the pharmaceutical composition;

b) a pharmaceutically-acceptable hydrophobic hard fat in an amount of about 30% to about 75% by weight of the pharmaceutical composition, the pharmaceutically-acceptable hydrophobic hard fat consisting of a mixture of saturated C 10 -C 18 triglycerides having a melting point range of 41° C. to 45° C.; and

c) a pharmaceutically-acceptable hydrophobic monoglyceride in an amount of about 8% to about 40% by weight of the pharmaceutical composition, the pharmaceutically-acceptable monoglyceride being liquid at 20° C.;

wherein the solid solution pharmaceutical composition does not comprise a pharmaceutically-acceptable hydrophilic solvent;

wherein the solid solution pharmaceutical composition is not a multi-phasic 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.

15. The solid solution pharmaceutical composition according to claim 14 , wherein the statin is in an amount of about 1% to 20% by weight of the pharmaceutical composition, the pharmaceutically-acceptable hard fat is in an amount of at least 50% by weight of the pharmaceutical composition and the pharmaceutically-acceptable monoglyceride is in an amount of less than 35% by weight of the pharmaceutical composition.

Assignments (4)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 13, 2016
From: BANNISTER, ROBIN M.; BREW, JOHN; CAPARROS-WANDERLEY, WILSON
To: BIOCOPEA LIMITED
Reel/Frame 038273/0815 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 23, 2015
From: REILEY, RICHARD ROBERT
To: BIOCOPEA LIMITED
Reel/Frame 035886/0079 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2014
From: BIOCOPEA LIMITED
To: IMMUNOCOPEA LIMITED
Reel/Frame 033743/0558 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 15, 2014
From: IMMUNOCOPEA LIMITED
To: INFIRST HEALTHCARE LIMITED
Reel/Frame 033743/0574 →
Priority Claims (5)
GB 1018289.7 · Oct 29, 2010 · national
GB 1101937.9 · Feb 4, 2011 · national
GB 1113728.8 · Aug 10, 2011 · national
GB 1113729.6 · Aug 10, 2011 · national
GB 1113730.4 · Aug 10, 2011 · national
Continuity (8)
Continuation In Part 13365824 · Feb 3, 2012
Continuation In Part PCTGB2011052115 · Oct 31, 2011
Continuation In Part 14155147
Continuation In Part 13365828 · Feb 3, 2012
Provisional Application 61752309 · Feb 4, 2013
Provisional Application 61752356 · Jan 14, 2013
Related Publication 20140128353A1 · May 8, 2014
Related Publication 20190083623A9 · Mar 21, 2019