Oral solid dosage forms containing a low dose of estradiol

• US 8,022,053 B2
• Filed: 11/01/2005
• Issued: 09/20/2011
• Est. Priority Date: 11/02/2004
• Status: Expired due to Fees

• Current Assignee: Bayer Schering Pharma AG (Bayer AG)
• Original Assignee: Bayer Schering Pharma AG (Bayer AG)
• Inventors: Wagner, Torsten, Mueller, Kristina, Funke, Adrian, Zurth, Christian
• Primary Examiner(s): Hui; San-Ming
• Assistant Examiner(s): ZAREK, PAUL E
• Application Number:
  US11/262,952
• Publication Number:
  US 20060111334A1
• Time in Patent Office: 2,149 Days
• Field of Search: 514/182
• US Class Current: 514/182
• CPC Class Codes: A61K 31/56 Compounds containing cyclopenta[a]hydrophenanthrene ring systems; Derivatives thereof, e.g. steroids
• CPC Class Codes: A61K 9/2009 Inorganic compounds
• CPC Class Codes: A61K 9/2018 Sugars, or sugar alcohols, e.g. lactose, mannitol; Derivatives thereof, e.g. polysorbates
• CPC Class Codes: A61K 9/2027 obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
• CPC Class Codes: A61K 9/2054 Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
• CPC Class Codes: A61K 9/2059 Starch, including chemically or physically modified derivatives; Amylose; Amylopectin; Dextrin
• CPC Class Codes: A61K 9/2813 Inorganic compounds
• CPC Class Codes: A61K 9/284 obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone
• CPC Class Codes: A61K 9/2866 Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose

Abstract

The present invention relates to oral solid dosage forms containing a very low dose of estradiol. The dosage forms are formulated in a manner so as to avoid degradation of the estradiol and to minimise the content of polyvinylpyrrolidone, while still achieving similar fast dissolution of the estradiol. The dosage forms are useful in preventing or treating a physical condition in a woman caused by insufficient endogenous levels of estradiol.

Claims

1. An oral solid dosage form comprising 0.05 mg to 0.2 mg of estradiol hemihydrate, and at least one pharmaceutically acceptable excipient, provided that the dosage form does not contain polyvinylpyrrolidone, and provided that the dosage form is in a form for oral administration.

2. The dosage form according to claim 1, wherein the estradiol hemihydrate is in micronised form.

3. The dosage form according to claim 1, wherein more than 70% of the estradiol hemihydrate is dissolved from the dosage form within 30 minutes as determined by USP 27 (Paddle System) using 900 ml of water at 37°

C. as the dissolution media and 50 rpm as the rotation speed.

4. The dosage form according to claim 3, wherein more than 80% of the estradiol hemihydrate is dissolved from the dosage form within 30 minutes.

5. The dosage form according to claim 4, wherein more than 90% of the estradiol hemihydrate is dissolved from the dosage form within 30 minutes.

6. The dosage form according to claim 1, wherein more than 70% of the estradiol hemihydrate is dissolved from the dosage form within 15 minutes as determined by USP 27 (Paddle System) using 900 ml of water at 37°

C. as the dissolution media and 50 rpm as the rotation speed.

7. The dosage form according to claim 6, wherein more than 80% of the estradiol hemihydrate is dissolved from the dosage form within 15 minutes.

8. The dosage form according to claim 1, wherein the oral solid dosage form comprises estradiol hemihydrate in an amount of from 0.1 mg to 0.2 mg.

9. The dosage form according to claim 8, wherein the oral solid dosage form comprises estradiol hemihydrate in an amount of from 0.15 mg to 0.2 mg.

10. The dosage form according to claim 9, wherein the oral solid dosage form comprises estradiol hemihydrate in an amount of 0.2 mg.

11. The dosage form according to claim 9, wherein the oral solid dosage form comprises estradiol hemihydrate in an amount of about 0.19 mg.

12. The dosage form according to claim 9, wherein the oral solid dosage form comprises estradiol hemihydrate in an amount of about 0.15 mg.

13. The dosage form according to claim 8, wherein the oral solid dosage form comprises estradiol hemihydrate in an amount of about 0.1 mg.

14. The dosage form according to claim 1, wherein at least 95% by weight of the initial amount of the estradiol hemihydrate is present in the dosage form following storage at 40°

C. and 75% relative humidity (RH) in darkness for 3 months.

15. The dosage form according to claim 1, wherein at least 85% by weight of the initial amount of the estradiol hemihydrate is present in the dosage form following storage at 40°

C. and 75% relative humidity (RH) in darkness for 12 months.

16. The dosage form according to claim 1, wherein the at least one pharmaceutically acceptable excipient is a binder selected from the group consisting of starch, starch derivatives, partly or fully modified or pregelatinized starch, cellulose, cellulose derivatives, and mixtures thereof.

17. The dosage form according to claim 16, wherein the binder is a cellulose derivative is selected from the group consisting of carboxymethylcellulose, ethyl cellulose, hydroxypropyl cellulose, hydroxyethylmethyl cellulose, hydroxypropylmethyl cellulose and methylcellulose.

18. The dosage form according to claim 17, wherein the cellulose derivative is hydroxypropyl cellulose.

19. The dosage form according to claim 1, wherein the dosage form does not contain an isoflavone.

20. The dosage form according to claim 1, wherein the dosage form does not contain a solubiliser.

21. The dosage form according to claim 1, wherein the dosage form does not contain a super disintegrant.

22. The dosage form according to claim 1, wherein the dosage form is in the form of a tablet, capsule, gelcap, granule, sachet or a pill.

23. The dosage form according to claim 22, wherein the dosage form is in the form of a tablet.

24. The dosage form according to claim 23, wherein the tablet is film-coated.

25. A process for manufacturing an oral solid dosage form of claim 1, comprising the steps of

a) providing a powdery mixture of estradiol hemihydrate;

b) granulating said powdery mixture into a granulate by adding a binder; and

optionally

c) mixing the resulting granulate with further pharmaceutically acceptable excipients; and

d) transforming the resulting mixture into a solid dosage unit form.