Dosing regimens for the treatment of lysosomal storage diseases using pharmacological chaperones
The present invention provides dosing regimens for administering pharmacological chaperones to a subject in need thereof. The dosing regimens can be used to treat disorders caused by improper protein misfolding, such as lysosomal storage disorders.
1 . A method of reducing globotriaosylceramide (GL-3) inclusion volume per podocyte in a patient having Fabry disease, the method comprising:
measuring the GL-3 inclusion volume per podocyte in the patient at baseline prior to administering to the patient a formulation comprising an effective amount of 1-deoxygalactonojirimycin or salt thereof;
administering to the patient a formulation comprising an effective amount of 1-deoxygalactonojirimycin or salt thereof every other day for at least 6 months, wherein the effective amount is about 123 mg free base equivalent (FBE); and
measuring the GL-3 inclusion volume per podocyte in the patient after 6 months of administering the formulation comprising an effective amount of 1-deoxygalactonojirimycin or salt thereof, wherein the GL-3 inclusion volume per podocyte is reduced after 6 months of administering the formulation comprising an effective amount of 1-deoxygalactonojirimycin or salt thereof.
2 . The method of claim 1 , wherein the 1-deoxygalactonojirimycin or salt thereof enhances α-galactosidase A activity.
3 . The method of claim 1 , wherein the patient is administered about 123 mg of 1-deoxygalactonojirimycin every other day.
4 . The method of claim 1 , wherein the patient is administered about 150 mg of migalastat hydrochloride every other day.
5 . The method of claim 1 , wherein the formulation comprises an oral dosage form.
6 . The method of claim 5 , wherein the oral dosage form comprises a tablet, a capsule or a solution.
7 . The method of claim 1 , further comprising reducing podocyte volume.