Isofagomine salts, methods of use and formulations
The present invention relates generally to the field of pharmaceuticals, and specifically relates to isofagomine (IFG), novel salts thereof and preparation methods and uses of these, for example, in formulating pharmaceutical compositions for the treatment of Gaucher disease. Also provided are novel crystalline forms of isofagomine salts, methods for preparing the crystalline forms, and their use in formulating pharmaceutical compositions.
1. A salt of isofagomine wherein the salt is selected from a quinate, maleate, fumarate, oxalate, malonate, succinate, cyclamate and ascorbate salt.
2. The salt according to claim 1 , wherein the salt is isofagomine quinate, isofagomine fumarate, isofagomine oxalate, isofagomine succinate, or isofagomine cyclamate.
3. The salt according to claim 2 , wherein isofagomine quinate is in a crystalline form characterized by an x-ray diffraction pattern having three or more characteristic peaks at 2theta values selected from: 9.5°±0.2°, 15.0°±0.2°, 17.4°±0.2°, 18.1°±0.2°, 20.3°±0.2°, 23.8°±0.2°, 24.8°±0.2° and 25.4°±0.2°; wherein isofagomine fumarate is in a crystalline form characterized by an x-ray diffraction pattern having three or more characteristic peaks at 2theta values selected from: 16.1°, ±0.2°, 18.3°, ±0.2°, 18.6°, ±0.2°, 21.9°, ±0.2°, 23.6°, ±0.2°, 23.8°±0.2° and 25.5°±0.2°; wherein isofagomine oxalate is in a crystalline form characterized by an x-ray diffraction pattern having three or more characteristic peaks at 2theta values selected from: 27.8°±0.2°, 32.2°±0.2°, 35.3°±0.2°, 36.6°±0.2°, 37.4°±0.2°, 38.4°±0.2°, 18.5°±0.2°, 19.2°±0.2°, 21.4°±0.2°, 22.6°±0.2°, 24.5°±0.2°, 24.8°±0.2°, 26.8°±0.2°, 20.2°±0.2° and 23.7°±0.2°; wherein isofagomine succinate is in a crystalline form characterized by having XRPD peaks; or wherein isofagomine cyclamate is in a crystalline form characterized by having XRPD peaks.
4. A salt of isofagomine wherein the salt is a crystalline form of isofagomine D-tartrate characterized by an x-ray diffraction pattern having three or more characteristic peaks at 2theta values selected from: 9.8°, ±0.2°, 10.5°±0.2°, 15°±0.2°, 15.3°±0.2°, 15.8°±0.2°, 17.4°±0.2°, 17.9°±0.2°, 18.5°±0.2°, 18.9°±0.2°, 19.6°±0.2°, 21.1°±0.2°, 21.7°±0.2°, 220° 0.2°, 24.2°±0.2°, 24.8°±0.2°, 26.6°±0.2°, 27.1°±0.2°, 27.4°±0.2°, 33.8°±0.2°, 35.7°±0.2°, 36.5°±0.2° and 37.5°±0.2°.
5. A pharmaceutical composition comprising at least one isofagomine salt according to claim 1 and a pharmaceutically acceptable carrier.
6. The pharmaceutical composition of claim 5 further comprising a glucocerebrosidase wherein isofagomine is present in an amount sufficient to stabilize the glucocerebrosidase.
7. The pharmaceutical composition of claim 5 , wherein the glucocerebrosidase is velaglucerase alfa.
8. The pharmaceutical composition of claim 5 , wherein the glucocerebrosidase and the isofagomine are in a molar ratio of about 1:2.5 to about 1:3.5.
9. The pharmaceutical composition of claim 8 , wherein the composition comprises 60-180 mg/mL of glucocerebrosidase and wherein isofagomine is present in at least about a 3-fold molar excess to the glucocerebrosidase.
10. The pharmaceutical composition of claim 6 , comprising glucocerebrosidase and isofagomine in a molar ratio of about 1:3, wherein the composition further comprises a sodium citrate buffer, sucrose and one or more surfactant selected from PS20, PS80 and poloxamer 188.
11. A method of preparing a pharmaceutical composition according to claim 5 comprising combining isofagomine and a pharmaceutically acceptable carrier.
12. A method of treating Gaucher disease, comprising administering to a patient in need of such a treatment a therapeutically effective amount of an isofagomine salt or formulation thereof according to claim 1 .
13. A method of producing an isofagomine salt comprising the steps of:
i) dissolving an organic acid in a polar protic solvent to produce a solution 1;
ii) dissolving isofagomine free base in a polar protic solvent to produce a solution 2;
iii) combining solution 1 and solution 2, thereby forming a precipitate; and
iv) isolating the precipitate corresponding to the isofagomine salt;
wherein the organic acid is selected from quinic acid, fumaric acid, oxalic acid, malonic acid, D-tartaric acid, L-tartaric acid, succinic acid, cyclamic acid and ascorbic acid.
14. A composition comprising an isofagomine salt according to claim 1 wherein the isofagomine salt is at least about 95% pure.
15. A method of treating Gaucher disease, comprising administering to a patient in need of such a treatment a therapeutically effective amount of a pharmaceutical composition according to claim 5 .
16. A method of treating Gaucher disease, comprising administering to a patient in need of such a treatment a therapeutically effective amount of an isofagomine salt or formulation thereof according claim 4 .
17. A method of treating Gaucher disease, comprising administering to a patient in need of such a treatment a therapeutically effective amount of a pharmaceutical composition according to claim 10 .
18. A pharmaceutical composition comprising at least one isofagomine salt according to claim 4 and a pharmaceutically acceptable carrier.