IP Library Granted Patent US 10,159,682
Granted Patent B2
US 10,159,682 · App. 15/211,094 · Granted Dec 25, 2018

Enzymatic process for obtaining 17 alpha-monoesters of cortexolone and/or its 9,11-dehydroderivatives

Inventors: Mauro Ajani (Lainate, IT); Luigi Moro (Cairate, IT)
Assignee: CASSIOPEA S.P.A.
A61K31/573A61K9/0014A61K9/06A61K47/06A61K47/10A61K47/14A61K47/26A61K47/44C07J5/0053C07J7/008C12P33/005C07B2200/13
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Quick Facts
Patent No.
US 10,159,682
App. No.
15/211,094
Granted
Dec 25, 2018
Kind
B2
Abstract

The present invention refers to a new enzymatic process for obtaining 17α-monoesters of cortexolone and/or its 9,11-dehydroderivatives starting from the corresponding 17α,21-diesters which comprises an enzymatic alcoholysis reaction. Furthermore, the present invention refers to new crystalline forms of cortexolone-17α-propionate and 9,11-dehydro-cortexolone 17α-butanoate.

Claims (24)

1. A method of treating a pathology affecting the skin and/or the cutaneous appendages, wherein the pathology affecting the skin and/or the cutaneous appendages is acne, androgenetic alopecia, hirsutism, or seborrheic dermatitis, the method comprising administering to a subject in need thereof an effective amount of crystalline form III of cortexolone-17α-propionate, wherein crystalline form III of cortexolone-17α-propionate is characterized by:

a DRX as shown in FIG. 7, 10 , or 13 ; or

a DRX with at least peaks at about: 6.2, 12.6, 14.1, 14.3, 16.0, 22.4, and 23.7 degrees 2theta.

2. The method of claim 1 , wherein crystalline form III of cortexolone-17α-propionate is applied topically.

3. The method of claim 2 , wherein the pathology affecting the skin and/or the cutaneous appendages is acne.

4. The method of claim 2 , wherein the pathology affecting the skin and/or the cutaneous appendages is androgenetic alopecia.

5. The method of claim 2 , wherein the pathology affecting the skin and/or the cutaneous appendages is hirsutism.

6. The method of claim 2 , wherein the pathology affecting the skin and/or the cutaneous appendages is seborrheic dermatitis.

7. A method of treating a pathology affecting the skin and/or the cutaneous appendages, wherein the pathology affecting the skin and/or the cutaneous appendages is acne, androgenetic alopecia, hirsutism, or seborrheic dermatitis, the method comprising administering to a subject in need thereof an effective amount of a composition comprising at least one physiologically acceptable excipient and crystalline form III of cortexolone-17α-propionate, wherein crystalline form III of cortexolone-17α-propionate is characterized by:

a DRX as shown in FIG. 7, 10 , or 13 ; or

a DRX with at least peaks at about: 6.2, 12.6, 14.1, 14.3, 16.0, 22.4, and 23.7 degrees 2theta.

8. The method of claim 7 , wherein the effective amount of the composition comprising at least one physiologically acceptable excipient and crystalline form III of cortexolone-17α-propionate is administered topically.

9. The method of claim 8 , wherein the pathology affecting the skin and/or the cutaneous appendages is acne.

10. The method of claim 8 , wherein the pathology affecting the skin and/or the cutaneous appendages is androgenetic alopecia.

11. The method of claim 8 , wherein the pathology affecting the skin and/or the cutaneous appendages is hirsutism.

12. The method of claim 8 , wherein the pathology affecting the skin and/or the cutaneous appendages is seborrheic dermatitis.

13. The method of claim 8 , wherein the at least one physiologically acceptable excipient is propylene glycol, cetylic alcohol, glyceryl monostearate, liquid paraffin, or a combination of any of the foregoing.

14. The method of claim 7 , wherein the composition is in the form of a tablet, capsule, powder, pellet, suspension, emulsion, cream, gel, ointment, lotion, or paste.

15. The method of claim 14 , wherein the composition is a powder, suspension, emulsion, cream, gel, ointment, lotion, or past, and is applied topically.

16. The method of claim 7 , wherein the composition further comprises solubilized cortexolone-17α-propionate.

17. The method of claim 16 , wherein the solubilized cortexolone-17α-propionate is present in the composition in a concentration of from 0.1 to 2% by weight of the composition.

18. The method of claim 16 , wherein the solubilized cortexolone-17α-propionate and crystalline form III of cortexolone-17α-propionate together comprise 0.1 to 2% by weight of the composition or comprise 0.2 to 1% by weight of the composition.

19. The method of claim 16 , wherein the composition further comprises any of crystalline forms I, II, or IV of cortexolone-17α-propionate, or any combination thereof, and wherein the solubilized cortexolone-17α-propionate and crystalline form III of cortexolone-17α-propionate together with any of crystalline forms I, II, or IV of cortexolone-17α-propionate, or any combination thereof, comprise 0.1 to 2% by weight of the composition or 0.2 to 1% by weight of the composition.

20. The method of claim 16 , wherein the composition further comprises any of crystalline forms I, II, or IV of cortexolone-17α-propionate, or any combination thereof, and wherein the solubilized cortexolone-17α-propionate and crystalline form III of cortexolone-17α-propionate together with any of crystalline forms I, II, or IV of cortexolone-17α-propionate, or any combination thereof, comprise 1% by weight of the composition.

Assignments (4)
CHANGE OF ADDRESS Recorded Sep 19, 2024
From: CASSIOPEA S.P.A.
To: CASSIOPEA S.P.A.
Reel/Frame 068999/0354 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2018
From: AJANI, MAURO; MORO, LUIGI
To: COSMO S.P.A.
Reel/Frame 047455/0017 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 8, 2018
From: COSMO S.P.A.
To: COSMO DERMATOS SRL
Reel/Frame 047455/0101 →
CHANGE OF NAME Recorded Nov 8, 2018
From: COSMO DERMATOS SRL
To: CASSIOPEA S.P.A.
Reel/Frame 047482/0675 →
Priority Claims (1)
IT MI2007A1616 · Aug 3, 2007 · national
Continuity (3)
Division 14073928 · Nov 7, 2013
Division 12671932
Related Publication 20160324873A1 · Nov 10, 2016
Cited By (1)
US 12,337,002