Orphi Therapeutics Inc — Department of Health and Human Services SBIR Phase I: 107

Description

DESCRIPTION provided by applicant Pharmacological Chaperone Therapy for the GM Gangliosidoses The ultimate goal of this application is the treatment of Tay Sachs Disease TSD and Sandhoff Disease SD collectively called the GM Gangliosidoses with the small molecule pharmacological chaperone OT Pharmacological chaperones PCs are small molecules that selectively bind and stabilize target proteins to facilitate proper folding reduce premature degradation and increase the efficiency of ER export This approach is broadly applicable to diseases where increasing the function of a specific protein mutant or wild type is predicted to provide therapeutic benefit OT is a potent hexosaminidase the deficient enzyme in these diseases targeted pharmacological chaperone with good bioavailability blood brain barrier penetration high selectivity for hexosaminidase and low cytotoxicity OT treatment increases levels of wild type and mutant hexosaminidase activity up to fold in cells and in wild type mouse brain tissue when orally administered Specifically OrPhi Therapeutics will determine the potency of OT for the R Q mutant form of hexosaminidase in a SD patient fibroblast cell line This will allow us to determine the dose range of OT that will need to be achieved when using a novel animal model in which the Hex B SD mutation R Q is expressed on a Hex background for pre clinical dosing studies This newly created mouse model is the only mouse model in which a pharmacological chaperone can be tested for dosing and possibly efficacy Additionally we intend to develop a cell based assay that discriminates between OT responsive and non responsive variants of Hex A and Hex B to determine which Tay Sachs and Sandhoff Disease patients will be amenable to pharmacological chaperone therapy with OT in future clinical trials The GM Gangliosidoses are life threatening neurodegenerative diseases for which no treatment is currently available The focus of this work is to provide pre clinical data to support the development of OT through IND enabling studies and subsequent clinical trials for the GM Gangliosidoses PUBLIC HEALTH RELEVANCE Tay Sachs disease and Sandhoff Disease or the GM Gangliosidoses are related genetic disorders that result from a deficiency of the enzyme beta hexosaminidase This enzyme catalyzes the degradation of glycoconjugates including gangliosides These diseases are rare diseases with severe central nervous system manifestations and currently there is no effective therapy This research could ultimately lead to an effective therapy for the GM Gangliosidoses