IP Library Granted Patent US 11,517,586
Granted Patent B2
US 11,517,586 · App. 17/471,111 · Granted Dec 6, 2022

Instructions for composition and sensitivity

Inventors: Yair Alster (Tel Aviv, IL); Charles Bosworth (Las Vegas, NV); Hila Epstein-Barash (Shoham, IL); Omer Rafaeli (Udim, IL)
Assignee: AZURA OPHTHALMICS LTD.
A61K33/04A61K9/0048A61K9/06A61P27/02
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Quick Facts
Patent No.
US 11,517,586
App. No.
17/471,111
Granted
Dec 6, 2022
Kind
B2
Abstract

Provided herein are methods treating a disease or disorder in or around the eye with a pharmaceutical composition comprising selenium disulfide (SeS 2 ) and instructing the treated individual to limit or avoid exposure to light following administration in order to reduce the adverse effect of the composition.

Claims (22)

1. A method for treating a disease or disorder in or around the eye in an individual in need thereof, the method comprising:

administering a therapeutically effective amount of a pharmaceutical composition to an ocular surface, surrounding ocular tissues, or a combination thereof of the individual;

wherein the pharmaceutical composition comprises a therapeutically effective amount of selenium disulfide (SeS 2 ); and

wherein the pharmaceutical composition is administered within an hour of bedtime or at nighttime.

2. The method of claim 1 , wherein the disease or disorder in or around the eye is meibomian gland dysfunction (MGD), blepharitis, seborrheic blepharitis, Demodex infestation, dry eye syndrome, hyperkeratosis, dermatitis, keratitis, contact lens discomfort, lid wiper epitheliopathy (LWE), Keratoconjunctivitis Sicca, Sjogren's Syndrome, or ocular rosacea.

3. The method of claim 2 , wherein the disease or disorder in or around the eye is Blepharitis or Seborrheic Blepharitis.

4. The method of claim 1 , wherein the pharmaceutical composition comprises selenium disulfide in a therapeutically effective concentration.

5. The method of claim 4 , wherein the therapeutically effective concentration is about 0.1 wt. % to about 10 wt. %.

6. The method of claim 1 , wherein the pharmaceutical composition is administered in a volume of less than 25 μL.

7. The method of claim 1 , wherein the pharmaceutical composition is a semi-solid, wherein the semi-solid is an ointment, a gel, a cream, or a paste.

8. The method of claim 1 , wherein the pharmaceutical composition is administered to the individual within an hour of bedtime.

9. The method of claim 1 , wherein the pharmaceutical composition is administered at nighttime.

10. The method of claim 1 , wherein the pharmaceutical composition is administered at dusk.

11. The method of claim 2 , wherein the disease or disorder in or around the eye is meibomian gland dysfunction (MGD).

12. The method of claim 2 , wherein the disease or disorder in or around the eye is dry eye syndrome.

13. The method of claim 2 , wherein the disease or disorder in or around the eye is keratitis or hyperkeratosis.

14. The method of claim 2 , wherein the disease or disorder in or around the eye is contact lens discomfort.

15. The method of claim 2 , wherein the disease or disorder in or around the eye is LWE.

16. The method of claim 1 , wherein the individual self-administers the pharmaceutical composition.

17. The method of claim 16 , wherein the pharmaceutical composition is applied with a finger.

18. The method of claim 16 , wherein the pharmaceutical composition is administered at home.

19. The method of claim 1 , wherein the pharmaceutical composition is administered after 4:00 PM.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 14, 2021
From: ALSTER, YAIR; BOSWORTH, CHARLES; EPSTEIN-BARASH, HILA; RAFAELI, OMER
To: AZURA OPHTHALMICS LTD.
Reel/Frame 057799/0482 →
Continuity (3)
Continuation PCTIB2021000005 · Jan 7, 2021
Provisional Application 62959738 · Jan 10, 2020
Related Publication 20210401877A1 · Dec 30, 2021
Cited By (1)
US 12,697,352