IP Library › Granted Patent US 8,980,840
Granted Patent B2
US 8,980,840 · App. 13/144,203 · Granted Mar 17, 2015

Therapeutic modulation of vaginal epithelium boundary lubrication

Inventors: Edward R. Truitt, III (San Diego, CA); Benjamin Sullivan (San Diego, CA); David Sullivan (Boston, MA)
Assignees: Schepens Eye Research Institute; Lubris LLC
A61K9/0034A61K9/02A61K9/06A61K31/70A61K31/715A61K38/13A61K38/24A61K45/06A61K38/1709A61K38/1793A61K38/20
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Quick Facts
Patent No.
US 8,980,840
App. No.
13/144,203
Granted
Mar 17, 2015
Kind
B2
Abstract

The present invention relates to the management of vaginal health. In particular, the present invention relates to pharmaceutical compositions, and methods of use thereof, for treating diseases associated with compromised boundary lubrication at the vaginal epithelium.

Claims (15)

1. A method of treating decreased vaginal boundary lubrication or a disease or condition associated therewith or of improving vaginal boundary lubrication, the method comprising topically administering to a vaginal surface of a subject in need thereof a therapeutically effective amount of isolated or purified lubricin or a lubricating fragment, multimer, or homolog thereof sufficient to improve vaginal boundary lubrication.

2. The method of claim 1 , wherein the disease or condition associated with decreased vaginal boundary lubrication is vaginal atrophy, dyspareunia, Sjogren's syndrome, menopause, androgen deficiency, estrogen deficiency, estrogen replacement therapy, allergy, chronic inflammation, menopause, premature menopause, chemotherapy, breastfeeding, surgical removal of the ovaries before menopause, genital lichen sclerosis, vulvodynia, bacterial vaginosis, herpes, candida, psoriasis, contact dermatitis, condylomata, or side effects of medications and aging.

3. The method of claim 1 , wherein the lubricin or lubricating fragment, multimer, or homolog thereof is formulated in a gel, an aqueous osmotically balanced salt solution, a multiphasic emulsion, or a slow- or extended-release device.

4. The method of claim 1 , wherein the therapeutically effective amount of lubricin or lubricating fragment, multimer, or homolog thereof is in a concentration of 10-10,000 μg/mL.

5. The method of claim 1 , wherein the lubricin or lubricating fragment, multimer, or homolog thereof has an average molar mass of between 50 kDa and 400 kDa.

6. The method of claim 1 , wherein the lubricin or lubricating fragment, multimer, or homolog thereof is a recombinant lubricin, or lubricating fragment, multimer, or homolog thereof, or a purified naturally occurring lubricin or lubricating fragment, multimer, or homolog thereof.

7. The method of claim 1 , further comprising administering a therapeutic agent selected from the group consisting of an androgen, androgen analogue, selective androgen receptor modulator, selective estrogen receptor modulator, estrogen antagonist, aromatase inhibitor, antiprotease, proinflammatory cytokine antagonist, cytokine release inhibitor, anti-inflammatory cytokine, anti-inflammatory agent, NF-κB inhibitor, proteasome inhibitor, hyaluronic acid, neutral lipids, polar lipids, fatty acids, estrogen, estrogen analogue, oestradiol, progesterone, follicle stimulating hormone, luteinizing hormone, sodium hyaluronate, and nitric oxide.

8. The method of claim 7 , wherein said androgen or androgen analogue is a 17α-methyl-17β-hydroxy-2-oxa-5α-androstan-3-one derivative, a testosterone derivative, 4,5α-dihydrotestosterone derivative, a 17β-hydroxy-5α-androstane derivative containing a ring A unsaturation, a 19-nortestosterone derivative, a nitrogen-substituted androgen, or a combination thereof.

9. The method of claim 7 , wherein said selective androgen receptor modulator is an aryl-propionamide compound, a bicyclic hydantoin analogue, a quinoline analogue, or a tetrahydroquinoline analogue.

10. The method of claim 7 , wherein said proinflammatory cytokine antagonist is an anti-TNFα antibody, a soluble TNF α receptor, or an IL-1 receptor antagonist.

11. The method of claim 7 , wherein said anti-inflammatory agent is cyclosporine A, omega 3 fatty acids, or omega 6 fatty acids.

12. The method of claim 7 , wherein the composition comprises sodium hyaluronate or hyaluronic acid in a concentration of 10-100,000 μg/mL.

13. The method of claim 7 , wherein the composition comprises sodium hyaluronate or hyaluronic acid in a concentration of 500-5,000 μg/mL.

14. A method of providing lubrication during intercourse or promoting conception comprising topically administering to a vaginal surface, a penile surface, or a combination thereof an effective amount of an isolated or purified lubricin or a lubricating fragment, multimer, or homolog thereof sufficient to improve vaginal boundary lubrication.

15. A method of treating decreased vaginal boundary lubrication or a disease or condition associated therewith or of improving vaginal boundary lubrication, the method comprising topically administering to a vaginal surface of a subject in need thereof a therapeutically effective amount of isolated or purified lubricin or a lubricating fragment, multimer, or homolog thereof sufficient to improve vaginal boundary lubrication and a therapeutic agent selected from the group consisting of an androgen, androgen analogue, selective androgen receptor modulator, selective estrogen receptor modulator, aromatase inhibitor, antiprotease, cytokine release inhibitor, NF-κB inhibitor, proteasome inhibitor, neutral lipids, polar lipids, fatty acids, estrogen, estrogen analogue, oestradiol, progesterone, follicle stimulating hormone, luteinizing hormone, and nitric oxide.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 29, 2013
From: SINGULARIS, INC.
To: LUBRIS LLC
Reel/Frame 029712/0880 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2011
From: TRUITT, EDWARD R., III; SULLIVAN, BENJAMIN
To: SINGULARIS, INC.
Reel/Frame 027200/0904 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2011
From: SULLIVAN, DAVID A.
To: SCHEPENS EYE RESEARCH INSTITUTE
Reel/Frame 027200/0962 →
Continuity (3)
Provisional Application 61260402 · Nov 12, 2009
Provisional Application 61144344 · Jan 13, 2009
Related Publication 20120052077A1 · Mar 1, 2012