IP Library Granted Patent US 11,690,826
Granted Patent B2
US 11,690,826 · App. 17/873,540 · Granted Jul 4, 2023

Methods for treating demodex blepharitis using lotilaner formulations

Inventors: Bobak Robert Azamian (Newport Coast, CA); Douglas Michael Ackermann (Reno, NV); Shawn D. Hickok (Aliso Viejo, CA); Joseph G. Vehige (Irvine, CA)
Assignee: Tarsus Pharmaceuticals, Inc.
A61K31/422A61K9/0048A61K9/08A61K47/26A61P27/02A61P33/14
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Quick Facts
Patent No.
US 11,690,826
App. No.
17/873,540
Granted
Jul 4, 2023
Kind
B2
Abstract

Disclosed herein are methods for treating or preventing ophthalmic and dermatologic conditions in a patient, including ocular surface conditions such as blepharitis. The methods can include topically administering directly to an ocular surface of one or more eyes of a patient in need of treatment thereof an effective amount of an isoxazoline parasiticide, formamidine parasiticide, or other active ingredient, formulated into an ophthalmic composition, the ophthalmic composition further comprising a pharmaceutically acceptable vehicle. Compositions are also disclosed.

Claims (20)

1. A method for treating Demodex blepharitis, comprising topically administering directly to an ocular surface of one or more eyes of a human patient in need of treatment thereof an effective amount of an ophthalmic composition, wherein the ophthalmic composition comprises lotilaner and a pharmaceutically acceptable vehicle, and wherein the lotilaner is present at about 0.25% by weight with respect to the total weight of the composition administered.

2. The method of claim 1 , wherein the ophthalmic composition comprises an eye drop.

3. The method of claim 1 , wherein topically administering further comprises topically administering the ophthalmic composition at least once daily for at least about 4 weeks.

4. The method of claim 3 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

5. The method of claim 1 , wherein topically administering further comprises topically administering the ophthalmic composition at least twice daily for at least about 6 weeks.

6. The method of claim 5 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

7. The method of claim 1 , wherein topically administering further comprises topically administering the ophthalmic composition at least twice daily for at least about 90 days.

8. The method of claim 7 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

9. The method of claim 1 , wherein topically administering further comprises topically administering the ophthalmic composition at least three times daily for at least about 90 days.

10. The method of claim 9 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

11. A method for treating Meibomian gland dysfunction caused by Demodex infestation, comprising topically administering directly to one or more of the eye, eyelids, or eyelashes of a human patient in need of treatment thereof an effective amount of an ophthalmic composition, wherein the ophthalmic composition comprises lotilaner and a pharmaceutically acceptable vehicle, and wherein the lotilaner is present at about 0.25% by weight with respect to the total weight of the composition administered.

12. The method of claim 11 , wherein the ophthalmic composition comprises an eye drop.

13. The method of claim 11 , wherein topically administering further comprises topically administering the ophthalmic composition at least once daily for at least about 4 weeks.

14. The method of claim 13 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

15. The method of claim 11 , wherein topically administering further comprises topically administering the ophthalmic composition at least twice daily for at least about 6 weeks.

16. The method of claim 15 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

17. The method of claim 11 , wherein topically administering further comprises topically administering the ophthalmic composition at least twice daily for at least about 90 days.

18. The method of claim 17 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

19. The method of claim 11 , wherein topically administering further comprises topically administering the ophthalmic composition at least three times daily for at least about 90 days.

20. The method of claim 19 , wherein each administering further comprises topically administering between about 25 microliters and about 50 microliters of the ophthalmic composition to the patient.

Assignments (2)
PATENT SECURITY AGREEMENT Recorded Apr 19, 2024
From: TARSUS PHARMACEUTICALS, INC.
To: BIOPHARMA CREDIT PLC
Reel/Frame 067171/0968 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 24, 2023
From: AZAMIAN, BOBAK ROBERT; ACKERMANN, DOUGLAS MICHAEL; HICKOK, SHAWN D.; VEHIGE, JOSEPH G.
To: TARSUS PHARMACEUTICALS, INC.
Reel/Frame 063421/0216 →
Continuity (8)
Continuation 17099570 · Nov 16, 2020
Continuation 16221390 · Dec 14, 2018
Provisional Application 62746498 · Oct 16, 2018
Provisional Application 62689787 · Jun 25, 2018
Provisional Application 62626612 · Feb 5, 2018
Provisional Application 62615855 · Jan 10, 2018
Provisional Application 62599213 · Dec 15, 2017
Related Publication 20220354829A1 · Nov 10, 2022
Cited By (4)
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