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filingDate 2008-03-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 2010-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-2010523578-A
titleOfInvention Method for treating Fabry disease using a pharmacological chaperone
abstract The present invention provides a method for treating a Fabry disease patient by determining whether there is an improvement in a surrogate marker associated with Fabry disease after administration of a specific pharmacological chaperone of α-galactosidase A. The method includes administering an effective amount of 1-deoxygalactonojirimycin to an individual, wherein 1-deoxygalactonojirimycin is an amount effective to increase the activity of α-galactosidase A. To α-galactosidase A. The present invention is also a method for monitoring and increasing the therapeutic response of a Fabry disease patient after administration of a specific pharmacological chaperone of α-galactosidase A by assessing the effect on the cytoplasmic staining pattern of cells derived from the patient. Also provided is a method wherein detection of an intracellular staining pattern that is similar to an intracellular staining pattern from a healthy individual is an indication that the individual suffering from Fabry disease is a responder.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2016117754-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2019510030-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-7098529-B2
priorityDate 2007-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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