IP Library Granted Patent US 8,247,393
Granted Patent B2
US 8,247,393 · App. 11/889,976 · Granted Aug 21, 2012

Conjugated estrogen compositions, applicators, kits, and methods of making and use thereof

View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 8,247,393
App. No.
11/889,976
Granted
Aug 21, 2012
Kind
B2
Abstract

The present invention is directed to monophasic pharmaceutical compositions comprising a conjugated estrogen and a hydrophilic or lipophilic excipient. The present invention is also directed to kits and applicators comprising the pharmaceutical compositions. The invention is also directed to methods for treating menopausal conditions in a female comprising administration of the pharmaceutical compositions.

Claims (30)

1. A method of treating a menopausal condition in a female in need thereof, the method comprising administering to the female a single unit-dose of a monophasic pharmaceutical composition comprising a conjugated estrogen and a hydrophilic excipient,

wherein the composition has a viscosity greater than about 1 Poise and less than about 30,000 Poise,

wherein the conjugated estrogen comprises a combination of sodium estrone sulfate, sodium equilin sulfate, sodium 17α-dihydroequilin sulfate, sodium 17β-dihydroequilin sulfate, sodium 17α-estradiol sulfate, sodium 17β-estradiol sulfate, sodium equilenin sulfate, sodium 17α-dihydroequilenin sulfate, sodium 17β-dihydroequilenin sulfate, and sodium Δ8,9-dehydroestrone sulfate, and wherein the diffusion of estrone or equilin from the composition across human vaginal tissue is from about 30% to about 90% at 24 hours.

2. The method of claim 1 , wherein the method comprises transmucosal administration.

3. The method of claim 1 , wherein the composition is administered at least once daily for at least 2 consecutive days.

4. The method of claim 1 , wherein the composition is administered at least twice per week for at least 1 week.

5. The method of claim 1 , wherein the composition is administered (a) at least once daily for at least 7 consecutive days, followed by (b) at least twice per week for at least 2 weeks.

6. The method of claim 1 , wherein the composition is administered (a) at least once daily for 2 to 13 consecutive days, followed by (b) at least twice per week for at least 2 weeks.

7. The method of claim 1 wherein the menopausal condition is selected from the group consisting of vaginal dryness, pain during intercourse, increased risk of infections, inability to control urination (incontinence), increased frequency of urinary infections, vaginal atrophy, kraurosis vulvae, hot flashes and night sweats, fatigue, emotional changes (mood swings and changes in sexual interest), sleep disturbances (insomnia), drier skin and hair, increased growth of facial and body hair, aches and pains in the joints, headaches, palpitations (rapid, irregular heart beats), vaginal itching, osteoporosis, and generalized itching.

8. The method of claim 1 , which provides systemic treatment of the menopausal condition.

9. The method of claim 1 , wherein the diffusion of estrone or equilin from the composition across a cellulose acetate membrane is from about 60% to about 90% at 6 hours.

10. The method of claim 1 , wherein the diffusion of estrone or equilin from the composition across human vaginal tissue is from about 40% to about 90% at 24 hours.

11. The method of claim 1 , wherein an applicator comprises the single unit-dose.

12. The method of claim 11 , wherein the applicator is a vaginal applicator.

13. The method of claim 1 , wherein the method comprises vaginal administration.

14. The method of claim 1 , wherein the conjugated estrogen consists of a combination of sodium estrone sulfate, sodium equilin sulfate, sodium 17α-dihydroequilin sulfate, sodium 17β-dihydroequilin sulfate, sodium 17α-estradiol sulfate, sodium 17β-estradiol sulfate, sodium equilenin sulfate, sodium 17α-dihydroequilenin sulfate, sodium 17β-dihydroequilenin sulfate, and sodium Δ8,9-dehydroestrone sulfate.

15. The method of claim 1 , wherein the sodium estrone sulfate, sodium equilin sulfate, sodium 17α-dihydroequilin sulfate, sodium 17β-dihydroequilin sulfate, sodium 17α-estradiol sulfate, sodium 17β-estradiol sulfate, sodium equilenin sulfate, sodium 17α-dihydroequilenin sulfate, sodium 17β-dihydroequilenin sulfate, and sodium Δ8,9-dehydroestrone sulfate are synthetic conjugated estrogens.

16. The method of claim 1 , wherein the composition is substantially free of ethanol.

17. The method of claim 1 , wherein the single unit-dose is an amount of about 50 mg to about 7.5 g of the composition.

18. The method of claim 1 , wherein the single unit-dose is an amount of about 100 mg to about 1 g of the composition.

19. The method of claim 1 , wherein the single unit-dose is an amount of about 50 mg to about 500 mg of the composition.

20. The method of claim 1 , wherein the composition comprises about 0.1 mg to about 15 mg of the conjugated estrogen.

21. The method of claim 1 , wherein the conjugated estrogen is about 0.02% to about 5% of the total weight of the composition.

22. The method of claim 1 , wherein the composition has a viscosity greater than about 50 Poise and less than about 2,500 Poise.

23. The method of claim 1 , wherein the composition further comprises a pharmaceutically acceptable excipient selected from the group consisting of an alkaline agent, a stabilizer, an adhesion agent, a solvent, a surfactant, a humectant, a buffering agent, and combinations thereof.

24. The method of claim 23 , wherein the adhesion agent is a carbomer, hydroxypropylmethylcellulose, or a combination thereof.

25. The method of claim 1 , wherein the composition has a viscosity greater than about 90 Poise and less than about 2,000 Poise.

26. The method of claim 1 , wherein the diffusion of estrone or equilin from the composition across human vaginal tissue is from about 50% to about 90% at 24 hours.

27. The method of claim 1 , wherein the composition further comprises carbomer.

28. The method of claim 27 , wherein the hydrophilic excipient comprises water and glycerin.

Assignments (2)
CHANGE OF NAME Recorded May 19, 2010
From: DURAMED PHARMACEUTICALS, INC.
To: TEVA WOMEN'S HEALTH, INC.
Reel/Frame 024402/0984 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 9, 2007
From: AHMED, SALAH U.; SHAIK, MADHU SUDHAN; GUPTA, SANJEEV K.
To: DURAMED PHARMACEUTICALS, INC.
Reel/Frame 020093/0456 →