IP Library Granted Patent US 9,937,188
Granted Patent B2
US 9,937,188 · App. 14/216,464 · Granted Apr 10, 2018

Non-irritating testosterone emulsions

Inventors: John T. Trogden (Villa Park, CA); Adnan K. Salameh (Irvine, CA); Chetan P. Pujara (Irvine, CA); Anuradha V. Gore (Irvine, CA); Jaya Giyanani (Irvine, CA); Andrea S. Kim (Irvine, CA); Mayssa Attar (Placentia, CA); Ronald Bradford (Mission Viejo, CA); Rhett M. Schiffman (Laguna Beach, CA)
Assignee: Allergan, Inc.
A61K31/568A61K9/00A61K9/0048A61K9/107A61K31/569A61K31/5685A61K45/06A61K47/02A61K47/06A61K47/10A61K47/26A61K47/32A61K47/40A61K47/44
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Quick Facts
Patent No.
US 9,937,188
App. No.
14/216,464
Granted
Apr 10, 2018
Kind
B2
Abstract

Disclosed herein are emulsions comprising testosterone or related androgens, castor oil, cyclodextrin, Pemulen TR-2, Polyoxyl 40, and other ingredients. The compositions are useful for treating keratoconjunctivitis sicca and meibomian gland disease.

Claims (23)

1. A method of treating meibomian gland disease, the method comprising topical ocular administration of an emulsion composition, the composition comprising testosterone at a concentration of about 0.1% (w/w) or 0.3% (w/w); Castor oil at a concentration between about 0.10% (w/w) and about 5% (w/w); a cyclodextrin at a concentration between about 0.25% (w/w) and about 10% (w/w); a C10-30 alkyl acrylate crosspolymer at a concentration between about 0.01% (w/w) and about 5% (w/w); and Polyoxyl 40 stearate at a concentration between about 0.01% (w/w) and about 5% (w/w).

2. The method of claim 1 , wherein the castor oil is present in the composition at a concentration of between about 0.10% (w/w) and about 1% (w/w).

3. The method of claim 2 , wherein the castor oil is present in the composition at a concentration of between about 0.10% (w/w) and about 0.5% (w/w).

4. The method of claim 3 , wherein the castor oil is present in the composition at a concentration of about 0.25% (w/w).

5. The method of claim 4 , wherein the cyclodextrin is sulfobutyl ether-β-cyclodextrin present in the composition at a concentration of between about 0.25% (w/w) and about 5% (w/w).

6. The method of claim 5 , wherein the sulfobutyl ether-β-cyclodextrin is present in the composition at a concentration of between about 0.25% (w/w) and about 5% (w/w).

7. The method of claim 6 , wherein the sulfobutyl ether-β-cyclodextrin is present in the composition at a concentration of about 0.36% (w/w), 1.25% (w/w), or about 3.75% (w/w).

8. The method of claim 7 , wherein the C10-30 alkyl acrylate crosspolymer is present in the composition at a concentration of between about 0.01% (w/w) and about 1% (w/w).

9. The method of claim 8 , wherein the C10-30 alkyl acrylate crosspolymer is present in the composition at a concentration of about 0.1% (w/w).

10. The method of claim 9 , wherein the Polyoxyl 40 stearate is present in the composition at a concentration of between about 0.01% (w/w) and about 2% (w/w).

11. The method of claim 10 , wherein the Polyoxyl 40 stearate is present in the composition at a concentration of between about 0.01% (w/w) and about 1% (w/w).

12. The method of claim 11 , wherein the Polyoxyl 40 stearate is present in the composition at a concentration of about 0.25% (w/w).

13. The method of claim 12 , wherein the composition further comprises Polysorbate 80 at a concentration of between about 0.01% (w/w) and about 5% (w/w).

14. The method of claim 13 , wherein the Polysorbate 80 is present in the composition at a concentration of between about 0.01% (w/w) and about 1% (w/w).

15. The method of claim 14 , wherein the Polysorbate 80 is present in the composition at a concentration of about 0.25% (w/w).

16. The method of claim 15 , wherein the composition further comprises glycerin at a concentration of between about 0.1% (w/w) and about 10% (w/w).

17. The method of claim 16 , wherein the glycerin is present in the composition at a concentration of between about 0.1% (w/w) and about 5% (w/w).

18. The method of claim 16 , wherein the glycerin is at a concentration of about 1.0% (w/w) or 1.5% (w/w).

19. The method of claim 18 , wherein the composition further comprises boric acid.

20. The method of claim 19 , wherein the composition further comprises sodium hydroxide.

21. The method of claim 20 , wherein the composition further comprises water.

22. The method of claim 1 , wherein the testosterone is present in the composition in a concentration of about 0.1% (w/w).

23. The method of claim 1 , wherein the testosterone is present in the composition in a concentration of about 0.3% (w/w).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 30, 2014
From: TROGDEN, JOHN T.; SALAMEH, ADNAN K.; PUJARA, CHETAN P.; GORE, ANURADHA V.; GIYANANI, JAYA; KIM, ANDREA S.; ATTAR, MAYSSA; BRADFORD, RONALD R.; SCHIFFMAN, RHETT M.
To: ALLERGAN, INC.
Reel/Frame 032788/0642 →
Continuity (4)
Continuation In Part 13357779 · Jan 25, 2012
Provisional Application 61436274 · Jan 26, 2011
Provisional Application 61800621 · Mar 15, 2013
Related Publication 20140315872A1 · Oct 23, 2014