IP Library Granted Patent US 11,844,836
Granted Patent B2
US 11,844,836 · App. 17/072,923 · Granted Dec 19, 2023

Topical pharmaceutical composition based on semifluorinated alkanes

Inventors: Bernhard Gunther (Dossenheim, DE); Bastian Theisinger (Mannheim, DE); Sonja Theisinger (Mannheim, DE); Dieter Scherer (Laufen, CH)
Assignee: DERMALIQ THERAPEUTICS, INC.
A61K45/06A61K9/0014A61K9/08A61K9/1075A61K31/355A61K31/436A61K47/06
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Quick Facts
Patent No.
US 11,844,836
App. No.
17/072,923
Granted
Dec 19, 2023
Kind
B2
Abstract

The invention provides liquid or semi-solid pharmaceutical compositions for topical administration comprising a semifluorinated alkane. The compositions are useful for the delivery of active ingredients into the deep layers of the skin or skin appendages. Various active ingredients may be incorporated, such as immunosuppressants, antiinfectives, antifungal agents, antiinflammatory agents, and retinoids.

Claims (15)

1. A method for treating a disease or condition affecting the layers of the skin below the stratum corneum, comprising administering a pharmaceutical composition comprising an effective amount of an active ingredient and a semifluorinated alkane according to formula

RFRH

wherein RF is a linear perfluorinated hydrocarbon segment with 4 to 12 carbon atoms, and RH is a linear alkyl group with 4 to 8 carbon atoms, and wherein the composition is to be topically administered to the skin; wherein the disease or condition affecting the layers of the skin below the stratum corneum is acne; and

wherein the active ingredient is selected from azithromycin, erythromycin, clindamycin, or minocycline.

2. The method of claim 1 , wherein the semifluorinated alkane is selected from F4H5, F4H6, F4H8, F6H6 and F6H8, wherein F means a perfluorinated hydrocarbon segment, H means a non-fluorinated segment, and the number is the number of carbon atoms of the respective segment.

3. The method of claim 1 , wherein the composition is in the form of a liquid or semisolid solution.

4. The method of claim 1 , wherein the composition comprises a physiologically acceptable cosolvent.

5. The method of claim 1 , wherein the disease or condition affects the vital epidermis, dermis, and/or hypodermis of the skin.

6. The method of claim 1 , wherein the active ingredient is azithromycin.

7. The method of claim 2 , wherein the semifluorinated alkane is selected from F4H5, F4H6, F6H6 and F6H8.

8. The method of claim 7 , wherein the semifluorinated alkane is F6H8.

9. The method of claim 1 , wherein the active ingredient penetrates through the stratum corneum and is delivered to layers of the skin below the stratum corneum.

10. The method of claim 9 , wherein the active ingredient is delivered to the viable epidermis, the dermis and/or the hypodermis.

11. The method of claim 4 , wherein the physiologically acceptable co-solvent is selected from ethanol, acetone, ethyl acetate, isopropyl alcohol, glycerol, propylene glycol, pentylene glycol, polyethylene glycol, liquid paraffin, triglyceride oils, hydrofluorocarbons, and liquid mono- or diglycerides.

12. The method of claim 4 , wherein the composition is in the form of a solution or emulsion.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 24, 2022
From: NOVALIQ GMBH
To: DERMALIQ THERAPEUTICS, INC.
Reel/Frame 059087/0281 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 28, 2021
From: GÜNTHER, BERNHARD; THEISINGER, BASTIAN; THEISINGER, SONJA; SCHERER, DIETER
To: NOVALIQ GMBH
Reel/Frame 057955/0030 →
Priority Claims (2)
EP 11167552 · May 25, 2011 · regional
EP 11167732 · May 26, 2011 · regional
Continuity (3)
Continuation 15721259 · Sep 29, 2017
Division 14122044
Related Publication 20210100904A1 · Apr 8, 2021
Cited By (5)
US 12,397,039 US 12,419,933 US 12,496,326 US 12,569,452 US 12,599,607