Pharmaceutical compositions comprising an aromatse inhibitors

1. A pharmaceutical composition, in the form of a capsule, comprising a blended mixture comprising

(a) a therapeutically effective amount of 4,4′-[fluoro-(1-H-1,2,4-triazol-1-yl)methylene] bisbenzonitrile which amount is from about 0.01 to about 3 mg per capsule;

(b) one or more filler;

(c) one or more disintegrant;

(d) one or more lubricant, and

(e) one or more glidant.

2. A pharmaceutical composition according to claim 1 , wherein said therapeutically effective amount of 4,4′-[fluoro-(1-H-1,2,4-triazol-1-yl)methylene]bisbenzonitrile is about 0.01 mg, about 0.05 mg, about 0.1 mg, about 0.3 mg, about 0.5 mg, about 1 mg, about 2 mg, or about 3 mg per capsule.

3. A pharmaceutical composition according to claim 1 , wherein said filler is selected from one or more of microcrystalline cellulose; low-substituted hydroxypropyl cellulose; hydroxyethyl cellulose; hydroxypropyl methyl cellulose; sugars, sugar alcohols, starches, starch derivatives; tricalcium phosphate, calcium hydrogen phosphate, calcium sulfate, dibasic calcium phosphates, and magnesium oxide.

4. A pharmaceutical composition according to claim 1 , wherein said filler is selected from one or more of microcrystalline cellulose, lactose, and maize starch.

5. A pharmaceutical composition according to claim 1 , wherein said disintegrant is selected from one or more of carboxymethylcellulose calcium (CMC-Ca), carboxymethylcellulose sodium (CMC-Na), crosscarmellose sodium, Sodium Starch Glycolate, alginic acid, sodium alginate and guar gum.

6. A pharmaceutical composition according to claim 1 , wherein said lubricant is selected from one or more of magnesium stearate, aluminium silicate, calcium silicate, stearic acid, cutina, PEG 4000-8000, and talc.

7. A pharmaceutical composition according to claim 1 , wherein said glidant is selected from one or more of colloidal silicon dioxide, magnesium trisilicate, powdered cellulose, starch, and talc.

8. A method for preparing a pharmaceutical composition according to claim 1 comprising the steps of:

(a) sequentially adding two portions of one or more filler and one portion of the therapeutic compound 4,4′-[fluoro-(1-H-1,2,4-triazol-1-yl)methylene] bisbenzonitrile (CGP47645) in the order first portion filler, therapeutic compound, second portion filler into a suitable mixing vessel and mixing the layers of the components using a suitable mixer to produce a pre-mix,

(b) sieving the pre-mix through a sieve with a mesh size of not more than 1.0 mm, preferably a mesh size of 0.5 mm,

(c) optionally mixing the sieved pre-mix using a suitable mixer,

(d) sieving a mixture of the remaining excipients, except the lubricant, through a sieve with a mesh size of not more than 1.0 mm, preferably a mesh size of 0.5 mm,

(e) mixing the pre-mix with the mixture of the remaining excipients, except the lubricant, using a suitable mixer,

(f) sieving the resulting mixture through a sieve with a mesh size of not more than 1.0 mm,

(g) optionally mixing the sieved mixture using a suitable mixer,

(h) sieving the lubricant, through a sieve with a mesh size of not more than 1.0 mm, and subsequently adding the lubricant to the resulting mixture of step (f) or (g),

(i) mixing the resulting mixture using a suitable mixer to obtain the final blend, and

(j) filling the final blend of step (i) into capsules, optionally using a suitable capsule filling machine.

9. A method of using the pharmaceutical composition of claim 1 in the treatment of a condition or disorder associated with aromatase activity.

10. The pharmaceutical composition of claim 5 wherein said disintegrant is Sodium Starch Glycolate.

11. The pharmaceutical composition of claim 6 wherein said lubricant is magnesium stearate.

12. The pharmaceutical composition of claim 6 wherein said glidantis colloidal silicon dioxide.

13. A pharmaceutical composition according to claim 1 , wherein

said filler is selected from the group consisting of microcrystalline cellulose, lactose and maize starch, and mixtures thereof,

said disintegrant is Sodium Starch Glycolate (SSG),

said lubricant is magnesium stearate, and

said glidant is colloidal silicon dioxide.

14. A pharmaceutical composition according to claim 1 wherein

said filler is employed in an amount ranging from about 80% to about 96% by weight of the capsule content,

said disintegrant is employed in an amount ranging from about 3% to about 6% by weight of the capsule content,

said lubricant is employed in an amount ranging from about 0.25% to about 5% by weight of the capsule content, and

said glidant is employed in an amount ranging from about 0.25% to about 1% by weight of the capsule content.

15. A pharmaceutical composition of claim 1 wherein said therapeutically effective amount of 4,4′-[fluoro-(1-H-1,2,4-triazol-1-yl)methylene]bisbenzonitrile is from 0.1 mg to 1.0 mg per capsule.

16. A pharmaceutical composition of claim 13 wherein said therapeutically effective amount of 4,4′-[fluoro-(1-H-1,2,4-triazol-1-yl)methylene]bisbenzonitrile is from 0.1 mg to 1.0 mg per capsule.

17. A pharmaceutical composition of claim 16 wherein said filler is a mixture of microcrystalline cellulose, lactose and maize starch.