IP Library Granted Patent US 9,872,901
Granted Patent B2
US 9,872,901 · App. 15/063,088 · Granted Jan 23, 2018

Therapeutic compositions for treatment of ocular inflammatory disorders

Inventors: Reza Dana (Newton, MA); Sunil Chauhan (Cambridge, MA)
Assignee: The Schepens Eye Research Institute, Inc.
A61K39/3955A61K9/0048A61K9/0051A61K31/724A61K31/728A61K38/1793A61K38/20A61K45/06C07K14/54C07K16/244C07K16/2866A61K2039/505C07K2317/75C07K2317/76
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,872,901
App. No.
15/063,088
Granted
Jan 23, 2018
Kind
B2
Abstract

The invention comprises a composition with means to inhibit the function of the inflammatory cytokine IL-17 and methods for using this composition to treat IL-17-mediated ocular inflammatory disorders. The invention also discloses devices for delivering this composition to the eye.

Claims (42)

1. A method for reducing the severity of dry eye syndrome comprising

identifying a subject characterized as suffering from dry eye syndrome;

topically administering directly to an eye of a subject a composition that inhibits binding of an inflammatory interleukin-17 (IL-17) cytokine to an IL-17 receptor; and

inhibiting or reducing eye dryness associated with said dry eye syndrome,

thereby reducing the severity of said dry eye syndrome, wherein said dry eye syndrome is caused by bone marrow transplant.

2. The method of claim 1 , wherein said identifying step comprises detection of a sign or symptom selected from the group consisting of eye dryness, scratching, stinging, itching, burning, irritation, pain, redness, inflammation, discharge, and excessive watering, and wherein said method inhibits or reduces the severity of at least one of said signs or symptoms.

3. The method of claim 1 , wherein said method comprises sequential or simultaneous administration of a composition that inhibits binding of an inflammatory IL-17 cytokine to an IL-17 receptor and a secondary composition.

4. The method of claim 1 , wherein the form of said composition is a solid, an ointment, a gel, a liquid, an aerosol, a mist, a polymer, a contact lens, a film, an emulsion, or a suspension.

5. The method of claim 1 , wherein said method does not comprise systemic administration or substantial dissemination to non-ocular tissue.

6. The method of claim 1 , wherein said composition further comprises a compound selected from the group consisting of a physiologically acceptable salt, poloxamer analogs with carbopol, carbopol/HPMC, carbopol-methyl cellulose, a mucolytic agent, carboxymethylcellulose (CMC), hyaluronic acid, cyclodextrin, and petroleum.

7. The method of claim 1 , wherein said method comprises administration of both a composition that inhibits binding of an inflammatory IL-17 cytokine to an IL-17 receptor and a second composition comprising one or more inflammatory antagonist(s).

8. The method of claim 1 , wherein said composition comprises:

(a) a monoclonal or polyclonal antibody;

(b) an antibody that targets an intracellular or extracellular IL-17 cytokine or IL-17 receptor;

(c) an antibody that binds to at least one intracellular or extracellular sequence of an IL-17 cytokine or IL-17 receptor;

(d) a single-chain antibody;

(e) a humanized, recombinant, or chimeric antibody;

(f) an antibody conjugated directly or indirectly to a compound that inhibits or modifies the activity of an IL-17 cytokine or an IL-17 receptor or

(g) a composition that inhibits or modifies the transcription, transcript stability, translation, modification, localization, secretion, or function of a polynucleotide or polypeptide encoding an inflammatory interleukin-17 cytokine or an IL-17 receptor.

9. The method of claim 1 , wherein said composition inhibits an activity of an inflammatory cytokine selected from the group consisting of IL-17A, IL-17B, IL-17C, IL-17D, IL-17E, and IL-17F.

10. The method of claim 1 , wherein said composition inhibits an activity of an inflammatory cytokine receptor selected from the group consisting of IL-17RA, IL-17RB, IL-17RC, IL-17RD, IL-17RE, and IL-17RF.

11. A method for reducing the severity of dry eye syndrome comprising

identifying a subject characterized as suffering from dry eye syndrome;

topically administering directly to an eye of a subject a composition that inhibits binding of an inflammatory interleukin-17 (IL-17) cytokine to an IL-17 receptor; and

inhibiting or reducing eye dryness associated with said dry eye syndrome,

thereby reducing the severity of said dry eye syndrome, wherein said subject has or has been subjected to a bone marrow transplant.

12. The method of claim 11 , wherein said identifying step comprises detection of a sign or symptom selected from the group consisting of eye dryness, scratching, stinging, itching, burning, irritation, pain, redness, inflammation, discharge, and excessive watering, and wherein said method inhibits or reduces the severity of at least one of said signs or symptoms.

13. The method of claim 11 , wherein said method comprises sequential or simultaneous administration of a composition that inhibits binding of an inflammatory IL-17 cytokine to an IL-17 receptor and a secondary composition.

14. The method of claim 11 , wherein the form of said composition is a solid, an ointment, a gel, a liquid, an aerosol, a mist, a polymer, a contact lens, a film, an emulsion, or a suspension.

15. The method of claim 11 , wherein said method does not comprise systemic administration or substantial dissemination to non-ocular tissue.

16. The method of claim 11 , wherein said composition further comprises a compound selected from the group consisting of a physiologically acceptable salt, poloxamer analogs with carbopol, carbopol/HPMC, carbopol-methyl cellulose, a mucolytic agent, carboxymethylcellulose (CMC), hyaluronic acid, cyclodextrin, and petroleum.

17. The method of claim 11 , wherein said method comprises administration of both a composition that inhibits binding of an inflammatory IL-17 cytokine to an IL-17 receptor and a second composition comprising one or more inflammatory antagonist(s).

18. The method of claim 11 , wherein said composition comprises:

(a) a monoclonal or polyclonal antibody;

(b) an antibody that targets an intracellular or extracellular IL-17 cytokine or IL-17 receptor;

(c) an antibody that binds to at least one intracellular or extracellular sequence of an IL-17 cytokine or IL-17 receptor;

(d) a single-chain antibody;

(e) a humanized, recombinant, or chimeric antibody;

(f) an antibody conjugated directly or indirectly to a compound that inhibits or modifies the activity of an IL-17 cytokine or an IL-17 receptor or

(g) a composition that inhibits or modifies the transcription, transcript stability, translation, modification, localization, secretion, or function of a polynucleotide or polypeptide encoding an inflammatory interleukin-17 cytokine or an IL-17 receptor.

19. The method of claim 11 , wherein said composition inhibits an activity of an inflammatory cytokine selected from the group consisting of IL-17A, IL-17B, IL-17C, IL-17D, IL-17E, and IL-17F.

20. The method of claim 11 , wherein said composition inhibits an activity of an inflammatory cytokine receptor selected from the group consisting of IL-17RA, IL-17RB, IL-17RC, IL-17RD, IL-17RE, and IL-17RF.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 8, 2016
From: DANA, REZA; CHAUHAN, SUNIL
To: THE SCHEPENS EYE RESEARCH INSTITUTE, INC.
Reel/Frame 037918/0859 →
Continuity (3)
Continuation 12812084
Provisional Application 61010566 · Jan 9, 2008
Related Publication 20160361412A1 · Dec 15, 2016