IP Library Granted Patent US 9,849,084
Granted Patent B2
US 9,849,084 · App. 15/205,390 · Granted Dec 26, 2017

Orally administered corticosteroid compositions

Inventors: Stephen Perrett (Princeton, NJ); Fredric Jay Cohen (Washington Crossing, PA); Gopi Venkatesh (Vandalia, OH)
Assignee: ADARE PHARMACEUTICALS, INC.
A61K9/0065A61K9/006A61K9/0053A61K9/0056A61K9/08A61K31/56A61K31/569A61K31/58A61K45/06A61K47/38A61K9/06
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Quick Facts
Patent No.
US 9,849,084
App. No.
15/205,390
Granted
Dec 26, 2017
Kind
B2
Abstract

The present invention is directed to orally administered corticosteroid compositions. The present invention also provides a method for treating a condition associated with inflammation of the gastrointestinal tract in an individual. The method comprises administering to an individual in need thereof a pharmaceutical composition of the present invention.

Claims (21)

1. An oral, liquid pharmaceutical composition comprising budesonide, a pharmaceutically acceptable liquid, and a phase change agent dissolved or suspended in the pharmaceutically acceptable liquid, wherein after oral administration to a patient, said composition undergoes a change in physical properties of the composition upon contact with the upper gastrointestinal tract of said patient, whereby contact of the corticosteroid with the upper gastrointestinal tract of the patient is enhanced and/or prolonged.

2. The liquid pharmaceutical composition of claim 1 , wherein the budesonide is suspended in the pharmaceutically acceptable liquid.

3. The liquid pharmaceutical composition of claim 1 , wherein the pharmaceutically acceptable liquid is selected from the group consisting of water, pharmaceutically acceptable alcohols, oils, glycols, glycol ethers, pyrrolidones, polyethylene glycols, N-methyl-2-pyrrolidone, 2-pyrrolidone, glycerol, tetraglycol, glycerol formal, solketal, ethyl acetate, ethyl lactate, ethyl butyrate, dibutyl malonate, tributyl citrate, tri-n-hexyl acetylcitrate, diethyl succinate, diethyl glutarate, diethyl malonate, triethyl citrate, triacetin, tributyrin, diethyl carbonate, propylene carbonate, acetone, methyl ethyl ketone, dimethyl sulfoxide, dimethyl sulfone, tetrahydrofuran, caprolactam, N,N-diethyl-m-toluamide, 1-dodecylazacycloheptan-2-one, 1,3-dimethyl-3,4,5,6-tetrohydro-2(1H)-pyrimidinone, and combinations thereof.

4. The liquid pharmaceutical composition of claim 1 , wherein the liquid composition is an aqueous suspension or solution.

5. The liquid pharmaceutical composition of claim 1 , wherein after administration to a patient, said composition precipitates onto the mucosa of the gastrointestinal tract of the patient, whereby deposition of the corticosteroid onto the mucosa of the gastrointestinal tract is enhanced and/or prolonged.

6. The liquid pharmaceutical composition of claim 1 , wherein after administration to a patient, said composition forms a gel on contact with the mucosa of the gastrointestinal tract of the patient, whereby the deposition of the corticosteroid onto the mucosa of the gastrointestinal tract is enhanced and/or prolonged.

7. The liquid pharmaceutical composition of claim 1 , wherein after administration to a patient, said composition increases in viscosity upon contact with the mucosa of the gastrointestinal tract of the patient, whereby the residence time of the corticosteroid on the mucosa of the intestinal tract is prolonged.

8. The liquid pharmaceutical composition of claim 1 , wherein said phase change agent is a poorly water-soluble polymer.

9. The liquid pharmaceutical composition of claim 1 , wherein said phase change agent is a thermosensitive polymer whose aqueous viscosity changes in the range of about 15 to about 40° C.

10. The liquid pharmaceutical composition of claim 1 , wherein said phase change agent increases in viscosity upon contact with fluids of the oropharynx.

11. The liquid pharmaceutical composition of claim 1 , wherein said pharmaceutically acceptable liquid is water-miscible.

12. The liquid pharmaceutical composition of claim 1 , wherein said phase change agent is a bio-gelling polymer selected from the group consisting of polylactides, polyglycolides, polycaprolactones, polydioxannones, polycarbonates, polyhydroxybutyrates, polyalkyene oxalates, polyanhydrides, polyamides, polyesteramides, polyurethanes, polyacetals, polyketals, polyorthocarbonates, polyphosphazenes, polyhydroxyvalerates, polyalkylene succinates, poly(malic acid), poly(amino acids), chitin, chitosan, polyorthoesters, cellulose derivatives, cellulose esters, methacrylic acid and methacrylate polymers, and copolymers, terpolymers and mixtures thereof.

13. The liquid pharmaceutical composition of claim 12 , wherein said bio-gelling polymer is ethylcellulose.

14. The liquid pharmaceutical composition of claim 10 , wherein said increase in viscosity is at least 50%.

15. A method for treating an inflammatory condition of the upper gastrointestinal tract comprising orally administering to an individual in need thereof the oral, liquid pharmaceutical composition of claim 1 .

16. The method of claim 15 , wherein said inflammatory condition is eosinophilic esophagitis.

17. The method of claim 15 , wherein said inflammatory condition comprises inflammation of the glottis, epiglottis, tonsils, oropharynx, or esophagus.

18. The method of claim 15 , wherein said inflammatory condition is viral or bacterial pharyngitis.

19. The method of claim 15 , wherein said inflammatory condition is gastroesophageal reflux disease (GERD), non-erosive reflux disease (NERD) or erosive esophagitis.

20. The method of claim 15 , wherein the amount of budesonide administered is from about 0.01 mg to about 20 mg.

21. The method of claim 15 , wherein the amount of budesonide administered is about 20 mg.

Assignments (9)
CHANGE OF NAME Recorded Apr 19, 2021
From: ADARE PHARMACEUTICALS US, L.P.
To: ELLODI PHARMACEUTICALS, L.P.
Reel/Frame 055966/0656 →
CORRECTIVE ASSIGNMENT TO CORRECT THE APPLICATION NUMBER, PATENT ISSUE DATE AND THE TITLE PREVIOUSLY RECORDED AT REEL: 053228 FRAME: 0251. ASSIGNOR(S) HEREBY CONFIRMS THE ASSIGNMENT. Recorded Oct 5, 2020
From: ADARE DEVELOPMENT I, L.P.
To: ADARE PHARMACEUTICALS US, L.P.
Reel/Frame 054003/0694 →
RELEASE OF SECURITY INTEREST RECORDED AT REEL/FRAMES 037246/0313, 047807/0967, 053474/0276 Recorded Sep 22, 2020
From: BANK OF MONTREAL, AS COLLATERAL AGENT
To: ADARE PHARMACEUTICALS, INC.; ADARE DEVELOPMENT I, L.P.; ADARE PHARMACEUTICALS USA, INC.
Reel/Frame 053852/0697 →
CHANGE OF NAME Recorded Jul 16, 2020
From: ADARE DEVELOPMENT I, L.P.
To: ADARE PHARMACEUTICALS US, L.P.
Reel/Frame 053228/0251 →
SECURITY INTEREST Recorded Dec 18, 2018
From: ADARE DEVELOPMENT I, L.P.
To: BANK OF MONTREAL
Reel/Frame 047807/0967 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 4, 2018
From: ADARE PHARMACEUTICALS, INC.
To: ADARE DEVELOPMENT I, L.P,
Reel/Frame 047672/0450 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 4, 2017
From: PERRETT, STEPHEN; COHEN, FREDERIC JAY; VENKATESH, GOPI
To: EURAND, INC.
Reel/Frame 043202/0964 →
CHANGE OF NAME Recorded Aug 4, 2017
From: EURAND INCORPORATED
To: APTALIS PHARMATECH INC.
Reel/Frame 043202/0977 →
CHANGE OF NAME Recorded Aug 4, 2017
From: APTALIS PHARMATECH, INC.
To: ADARE PHARMACEUTICALS, INC.
Reel/Frame 043203/0001 →
Continuity (4)
Continuation 14311732 · Jun 23, 2014
Division 12896005 · Oct 1, 2010
Provisional Application 61247642 · Oct 1, 2009
Related Publication 20170071855A1 · Mar 16, 2017