IP Library Granted Patent US 11,628,155
Granted Patent B2
US 11,628,155 · App. 16/794,692 · Granted Apr 18, 2023

Method for therapeutic treatment of rosacea

Inventors: Ofer Toledano (Kfar Saba, IL); Ori Nov (Tarum, IL)
Assignee: SOL-GEL TECHNOLOGIES LTD.
A61K31/327A61K9/0014A61K9/06A61K9/10A61K9/107A61K9/50A61P17/00A61P17/10
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Quick Facts
Patent No.
US 11,628,155
App. No.
16/794,692
Granted
Apr 18, 2023
Kind
B2
Abstract

A regimen and a pharmaceutical composition for the treatment of rosacea are described. The regimen includes topically applying to the skin of a subject in need of such treatment a pharmaceutical composition comprising about 1% w/w to about 10% w/w benzoyl peroxide as an active ingredient, and the pharmaceutically acceptable carrier or excipient, where the benzoyl peroxide is the only active ingredient in the pharmaceutical composition, and the pharmaceutical composition is a cream or an emulsion.

Claims (57)

1. A regimen for the therapeutic treatment of rosacea, the regimen comprising topically applying to the skin of a subject in need of said treatment a pharmaceutical composition, the pharmaceutical composition comprising about 2.5% w/w to about 10% w/w benzoyl peroxide as an active ingredient, and a pharmaceutically acceptable carrier or excipient, wherein:

the benzoyl peroxide is the only active ingredient in said pharmaceutical composition;

the benzoyl peroxide is not encapsulated within a microcapsule or microsphere consisting of a metal oxide or a semi-metal oxide; and

said pharmaceutical composition comprises a fatty phase and/or an oily phase that forms a barrier between the benzoyl peroxide and its surrounding environment in the composition.

2. The regimen of claim 1 , wherein said pharmaceutical composition comprises about 2.5% w/w to about 5% w/w of benzoyl peroxide.

3. The regimen of claim 1 , wherein the benzoyl peroxide is not encapsulated within a microcapsule.

4. The regimen of claim 1 , wherein after the topical application, skin irritation of the subject, and the amount of benzoic acid in the dermis of the skin of the subject, are decreased, compared to skin irritation of the subject and the amount of benzoic acid in the dermis of the skin of the subject, respectively, after topical application of a corresponding pharmaceutical composition without the fatty phase and/or the oily phase.

5. The regimen of claim 1 , wherein an amount of benzoic acid in the stratum corneum and the epidermis of the skin of the subject after treatment with said pharmaceutical composition is higher than an amount of benzoic acid in the dermis of the skin of the subject after treatment with said pharmaceutical composition.

6. The regimen of claim 1 , wherein the benzoyl peroxide is the sole active ingredient administered to the subject during the duration of the regimen.

7. The regimen of claim 1 , wherein the pharmaceutical composition comprises about 5% w/w of benzoyl peroxide.

8. The regimen of claim 1 , wherein the benzoyl peroxide is selected from a solid, solution or suspension form.

9. The regimen of claim 1 , wherein the rosacea is any of erythematotelangiectatic rosacea, papulopustular rosacea, phymatous rosacea or ocular rosacea.

10. The regimen of claim 1 , wherein said pharmaceutical composition is an extended-release formulation.

11. The regimen of claim 10 , wherein the extended-release effect is obtained by encapsulation, microencapsulation, microspheres or coating.

12. The regimen of claim 1 , wherein irritation observed on the skin of the subject after treatment with said pharmaceutical composition remains constant over time.

13. The regimen of claim 10 , wherein the extended-release effect is obtained by the fatty phase and/or the oily phase that forms a barrier between the benzoyl peroxide and its surrounding environment in the composition.

14. The regimen of claim 1 , wherein the benzoyl peroxide is not encapsulated within a microcapsule comprising an inorganic polymer.

15. The regimen of claim 1 , wherein the pharmaceutical composition does not comprise a gelling agent.

16. The regimen of claim 1 , wherein:

the fatty phase and/or the oily phase is dispersed in an aqueous phase; or

the pharmaceutical composition comprises an aqueous phase dispersed in the fatty phase and/or the oily phase.

17. The regimen of claim 1 , wherein said pharmaceutical composition is a cream.

18. The regimen of claim 1 , wherein the irritation is reduced when evaluated on a 0-3 scale.

19. A regimen for the therapeutic treatment of rosacea, the regimen comprising topically applying to the skin of a subject in need of said treatment a pharmaceutical composition, the pharmaceutical composition comprising about 2.5% w/w to about 10% w/w benzoyl peroxide as an active ingredient, and a pharmaceutically acceptable carrier or excipient, wherein the benzoyl peroxide is encapsulated within a microcapsule and is the only active ingredient in said pharmaceutical composition, wherein said pharmaceutical composition is a cream, and wherein an amount of benzoic acid in the stratum corneum and the epidermis of the skin of the subject after treatment with said pharmaceutical composition is higher than an amount of benzoic acid in the dermis of the skin of the subject after treatment with said pharmaceutical composition.

20. The regimen of claim 19 , wherein the amount of benzoic acid in the stratum corneum and the epidermis of the skin of the subject is higher than the amount of benzoic acid in the dermis of the skin of the subject when measured by high-performance liquid chromatography (HPLC).

21. The regimen of claim 19 , wherein the amount of benzoic acid in the stratum corneum and the epidermis of the skin of the subject is higher than the amount of benzoic acid in the dermis of the skin of the subject when measured by HPLC about 24 hours following the application of the pharmaceutical composition to the skin of the subject.

22. The regimen of claim 19 , wherein the amount of benzoic acid in the stratum corneum and the epidermis of the skin of the subject is substantially higher than the amount of benzoic acid in the dermis of the skin of the subject after treatment with said pharmaceutical composition.

23. The regimen of claim 19 , wherein irritation observed on the skin of the subject after treatment with said pharmaceutical composition is reduced compared to after treatment with a corresponding pharmaceutical composition in which the benzoyl peroxide is not encapsulated within a microcapsule.

24. The regimen of claim 23 , wherein the irritation is reduced when evaluated on a 0-3 scale.

25. The regimen of claim 19 , wherein the microcapsule comprises an inorganic polymer.

26. The regimen of claim 19 , wherein the benzoyl peroxide is the sole active ingredient administered to the subject during the duration of the regimen.

27. The regimen of claim 19 , wherein the pharmaceutical composition comprises about 5% w/w of benzoyl peroxide.

28. The regimen of claim 19 , wherein the benzoyl peroxide is selected from a solid, solution or suspension form.

29. The regimen of claim 19 , wherein the rosacea is any of erythematotelangiectatic rosacea, papulopustular rosacea, phymatous rosacea or ocular rosacea.

30. The regimen of claim 19 , wherein said pharmaceutical composition is an extended-release formulation.

31. The regimen of claim 19 , wherein the pharmaceutical composition does not comprise a gelling agent.

32. The regimen of claim 19 , wherein irritation observed on the skin of the subject after treatment with said pharmaceutical composition remains constant over time.

33. A regimen for the therapeutic treatment of rosacea, the regimen comprising topically applying to the skin of a subject in need of said treatment a pharmaceutical composition, the pharmaceutical composition comprising about 2.5% w/w to about 10% w/w benzoyl peroxide as an active ingredient, and a pharmaceutically acceptable carrier or excipient, wherein the benzoyl peroxide is the only active ingredient in said pharmaceutical composition, wherein a total amount of benzoic acid in the skin of the subject after treatment with said pharmaceutical composition is less than about 18,333 ng/cm 2 , and wherein said pharmaceutical composition is a cream.

34. The regimen of claim 33 , wherein the amount of benzoic acid in the skin of the subject after treatment with said pharmaceutical composition ranges from about 6,667 ng/cm 2 to about 10,000 ng/cm 2 .

35. The regimen of claim 33 , wherein the amount of benzoic acid in the skin of the subject after treatment with said pharmaceutical composition ranges from about 7,500 ng/cm 2 to about 9,167 ng/cm 2 .

36. The regimen of claim 33 , wherein the benzoyl peroxide is not encapsulated within a microcapsule or a coating.

37. The regimen of claim 33 , wherein the benzoyl peroxide is encapsulated within a microcapsule or a coating.

38. The regimen of claim 37 , wherein the benzoyl peroxide is encapsulated within a microcapsule comprising an inorganic polymer.

39. The regimen of claim 33 , wherein the benzoyl peroxide is the sole active ingredient administered to the subject during the duration of the regimen.

40. The regimen of claim 33 , wherein the pharmaceutical composition comprises about 5% w/w of benzoyl peroxide.

41. The regimen of claim 33 , wherein the benzoyl peroxide is selected from a solid, solution or suspension form.

42. The regimen of claim 33 , wherein the rosacea is any of erythematotelangiectatic rosacea, papulopustular rosacea, phymatous rosacea or ocular rosacea.

43. The regimen of claim 33 , wherein said pharmaceutical composition is an extended-release formulation.

44. The regimen of claim 33 , wherein the pharmaceutical composition does not comprise a gelling agent.

45. The regimen of claim 33 , wherein irritation observed on the skin of the subject after treatment with said pharmaceutical composition remains constant over time.

46. The regimen of claim 33 , wherein irritation observed on the skin of the subject after treatment with said pharmaceutical composition is reduced compared to after treatment with a corresponding pharmaceutical composition that is not a cream.

47. The regimen of claim 46 , wherein the irritation is reduced when evaluated on a 0-3 scale.

48. The regimen of claim 36 , wherein irritation observed on the skin of the subject after treatment with said pharmaceutical composition is reduced compared to after treatment with a corresponding pharmaceutical composition that is not a cream.

49. The regimen of claim 48 , wherein the irritation is reduced when evaluated on a 0-3 scale.

50. The regimen of claim 37 , wherein irritation observed on the skin of the subject after treatment with said pharmaceutical composition is reduced compared to after treatment with a corresponding pharmaceutical composition that is not a cream.

51. The regimen of claim 50 , wherein the irritation is reduced when evaluated on a 0-3 scale.

52. The regimen of claim 1 , wherein the benzoyl peroxide is not encapsulated within a microcapsule or microsphere comprising a metal oxide or a semi-metal oxide.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 18, 2025
From: SOL-GEL TECHNOLOGIES LTD.
To: MAYNE PHARMA LLC
Reel/Frame 071148/0446 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 13, 2020
From: TOLEDANO, OFER; NOV, ORI
To: SOL-GEL TECHNOLOGIES LTD
Reel/Frame 052105/0200 →
Continuity (11)
Provisional Application 62977974 · Feb 18, 2020
Provisional Application 62977952 · Feb 18, 2020
Provisional Application 62972896 · Feb 11, 2020
Provisional Application 62972310 · Feb 10, 2020
Provisional Application 62960384 · Jan 13, 2020
Provisional Application 62925258 · Oct 24, 2019
Provisional Application 62871286 · Jul 8, 2019
Provisional Application 62871283 · Jul 8, 2019
Provisional Application 62807368 · Feb 19, 2019
Provisional Application 62807356 · Feb 19, 2019
Related Publication 20200261396A1 · Aug 20, 2020