IP Library Granted Patent US 7,569,557
Granted Patent B2
US 7,569,557 · App. 11/607,919 · Granted Aug 4, 2009

Compositions of estrogen-cyclodextrin complexes

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Quick Facts
Patent No.
US 7,569,557
App. No.
11/607,919
Granted
Aug 4, 2009
Kind
B2
Abstract

Pharmaceutical compositions comprising low doses of sensitive complexes between an estrogen and a cyclodextrin are provided with improved stability. In specific embodiments the composition comprises a complex between ethinyl estradiol and β-cyclodextrin in a granulate preparation and in yet another embodiment the composition comprises a limited amount of polyvinylpyrrolidone since this excipient was found to degrade ethinyl estradiol. Furthermore, a method for improving the stability of an estrogen in a composition and for manufacturing such a stable composition is provided. Essentially, the granulate preparation are manufactured under careful control of the relative humidity.

Claims (18)

1. A daily dosage unit for inhibiting ovulation comprising:

i) micronized drospirenone and a complex between ethinyl estradiol and a cyclodextrin, wherein drospirenone is present in an amount of from 2 mg to 4 mg, and wherein ethinyl estradiol is present in an amount of from 0.01 mg to 0.05 mg; and

ii) one or more excipients(s).

2. The dosage unit according to claim 1 , wherein ethinyl estradiol is present in an amount of from 0.015 mg to 0.04 mg.

3. The dosage unit of claim 1 , wherein the ethinyl estradiol is present in an amount of from 0.015 mg to 0.03 mg.

4. The dosage unit of claim 1 , wherein drospirenone is present in an amount of from 2.5 mg to 3.5 mg.

5. The dosage unit of claim 1 , wherein drospirenone is present in an amount of about 3 mg.

6. The dosage unit of claim 1 , wherein the cyclodextrin is selected from the group consisting of α-cyclodextrin, β-cyclodextrin, γ-cyclodextrin and alkylated or acylated derivatives thereof.

7. The dosage unit of claim 1 , wherein the cyclodextrin is selected from the group consisting of β-cyclodextrin and alkylated or acylated derivatives thereof.

8. The dosage unit of claim 1 , wherein the cyclodextrin is β-cyclodextrin.

9. The dosage unit of claim 1 , wherein the complex between ethinyl estradiol and a cyclodextrin is micronized.

10. The dosage unit of claim 1 , wherein the micronized drospirenone and the complex between ethinyl estradiol and a cyclodextrin are in the form of a granulate preparation having a relative humidity of at most 60%, as determined at a temperature between 20° C. and 40° C.

11. The dosage unit of claim 10 , wherein the granulate preparation has a relative humidity of at most 55%, as determined at a temperature between 20° C. and 40° C.

12. The dosage unit according to claim 1 , comprising, at most, 2% w/w of polyvinylpyrrolidone.

13. The dosage unit according to claim 1 , comprising, at most, 1% w/w of polyvinylpyrrolidone.

14. The dosage unit according to claim 1 , further comprising an antioxidant.

15. The dosage unit according to claim 1 , wherein the dosage unit is in the form of a tablet, capsule or sachet.

16. The dosage unit according to claim 1 , wherein the dosage unit is in the form of a tablet.

Assignments (2)
CHANGE OF NAME Recorded Jun 12, 2013
From: BAYER PHARMA AKTIENGESELLSCHAFT
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 030596/0431 →
CHANGE OF NAME Recorded Oct 11, 2011
From: BAYER SCHERING PHARMA AKTIENGESELLSCHAFT
To: BAYER PHARMA AKTIENGESELLSCHAFT
Reel/Frame 027046/0099 →