Methods for treatment of Fabry disease
Provided are in vitro and in vivo methods for determining whether a patient with Fabry disease will respond to treatment with a specific pharmacological chaperone.
1. A method for treatment of Fabry disease in a human patient in need thereof, the method comprising administering to the patient a therapeutically effective dose of 1-deoxygalactonojirimycin or a salt thereof every other day.
2. The method of claim 1 , wherein the 1-deoxygalactonojirimycin or salt thereof is administered as an oral dosage form.
3. The method of claim 2 , wherein the oral dosage form comprises a tablet, a capsule or a solution.
4. The method of claim 1 , wherein the patient does not eat food from about 2 hours before to about 2 hours after administering the 1-deoxygalactonojirimycin or salt thereof.
5. The method of claim 1 , wherein the 1-deoxygalactonojirimycin or salt thereof enhances α-galactosidase A activity.
6. The method of claim 1 , wherein the patient is male.
7. The method of claim 1 , wherein the patient is female.
8. The method of claim 1 , wherein the patient has an α-galactosidase A mutation selected from the group consisting of D244N, E59K, F113L, G144V, G183D, G328A, I91T, L32P, M284T, M296V, N263S, R363C, R363H, N34S, T41I, M51K, A97V, R112H, A143T, P205T, Y207S, N215S, P259R, N263S, L300P, E358A, P409A, S201F and F295C.
9. A method for treatment of Fabry disease in a human patient in need thereof, the method comprising administering to the patient a therapeutically effective dose of migalastat hydrochloride every other day.
10. The method of claim 9 , wherein the migalastat hydrochloride is administered as an oral dosage form.
11. The method of claim 10 , wherein the oral dosage form comprises a tablet, a capsule or a solution.
12. The method of claim 9 , wherein the patient does not eat food from about 2 hours before to about 2 hours after administering the migalastat hydrochloride.
13. The method of claim 9 , wherein the migalastat hydrochloride enhances α-galactosidase A activity.
14. The method of claim 9 , wherein the patient is male.
15. The method of claim 9 , wherein the patient is female.
16. The method of claim 9 , wherein the patient has an α-galactosidase A mutation selected from the group consisting of D244N, E59K, F113L, G144V, G183D, G328A, I91T, L32P, M284T, M296V, N263S, R363C, R363H, N34S, T41I, M51K, A97V, R112H, A143T, P205T, Y207S, N215S, P259R, N263S, L300P, E358A, P409A, S201F and F295C.