Methods and pharmaceutical composition for the treatment of inflammatory skin diseases associated with desmoglein-1 deficiency
US-2019125826-A1 · May 2, 2019 · US
US12544386B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12544386-B2 |
| Application number | US-202017610276-A |
| Country | US |
| Kind code | B2 |
| Filing date | May 13, 2020 |
| Priority date | May 15, 2019 |
| Publication date | Feb 10, 2026 |
| Grant date | Feb 10, 2026 |
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The present invention provides a method and a pharmaceutical composition for treatment of skin diseases associated with accelerated comeodesmosomes degradation and/or weaker cell-cell adhesion, such as a peeling skin syndrome, Netherton syndrome, and atopic dermatitis.
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The invention claimed is: 1 . A method for treatment of a skin disease or disorder associated with accelerated corneodesmosomes degradation and/or weaker cell-cell adhesion in a subject in need thereof, comprising administering/applying to the skin of said subject a topical pharmaceutical composition comprising a topically acceptable oily carrier and a therapeutically effective amount of an active agent selected from the group consisting of betulinic acid and a pharmaceutically acceptable salt, ester, or amide thereof, wherein said skin disease or disorder is peeling skin syndrome (PSS). 2 . The method of claim 1 , wherein said active agent is betulinic acid or a pharmaceutically acceptable salt thereof. 3 . The method of claim 1 , wherein said active agent is betulinic acid ester. 4 . The method of claim 1 , wherein said active agent is betulinic acid amide. 5 . The method of claim 1 , wherein said topical pharmaceutical composition is administered to one or more sites on the subject's skin. 6 . The method of claim 1 , wherein said topical pharmaceutical composition is administered once, twice, or thrice a day. 7 . The method of claim 1 , wherein said topical pharmaceutical composition is formulated as an ointment, salve, cream, paste, lotion, or oil-in-water emulsion. 8 . The method of claim 7 , wherein said topically acceptable oily carrier comprises at least one viscosity-modifying agent. 9 . The method of claim 8 , wherein said topically acceptable oily carrier comprises a paraffin oil and white petroleum. 10 . The method of claim 7 , wherein said topical pharmaceutical composition comprises up to about 20%, by weight, of said active agent. 11 . The method of claim 1 , wherein said subject does not suffer from epidermolysis bullosa, or from melanoma. 12 . The method of claim 8 , wherein said viscosity-modifying agent is a mineral oil or a surfactant. 13 . The method of claim 11 , wherein said epidermolysis bullosa is dystrophic epidermolysis bullosa or junctional epidermolysis bullosa, and said melanoma is cutaneous metastatic melanoma. 14 . The method of claim 1 , wherein said peeling skin syndrome (PSS) is noninflammatory PSS, inflammatory PSS, or acral PSS. 15 . The method of claim 1 , wherein said topical pharmaceutical composition is formulated as an ointment, and said active agent is betulinic acid. 16 . The method of claim 15 , wherein said PSS is noninflammatory PSS.
Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite · CPC title
Skin, i.e. galenical aspects of topical compositions (non-active ingredients are additionally classified in A61K47/00; A61K9/0009, A61K9/0021, A61K9/7015, A61K9/7023 take precedence; cosmetic preparations A61K8/00, A61Q; preparations for wound dressings or bandages A61L26/00) · CPC title
Drugs for dermatological disorders · CPC title
of carboxylic acids · CPC title
Carboxylic acids, e.g. valproic acid (salicylic acid A61K31/60) · CPC title
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