SPERAGEN, INC. — Department of Health and Human Services STTR Phase I: 102

SPERAGEN, INC. — STTR Phase I award from Department of Health and Human Services.

Amount
$223,095
Agency
Department of Health and Human Services · National Institutes of Health
Program / Phase
STTR · Phase I
Topic
102
Solicitation
PA17-303
NAICS
Place of performance
TX
Period
2018-08-01 → 2019-07-31

Description

SUMMARY Succinic semialdehyde dehydrogenase deficiencySSADHDis a rare neurometabolic disease caused by mutations in the ALDH AgeneThe disorder is associated with significant developmental delay and extensive neurological morbidity including seizuresSeizures increase with agein patients as well as in experimental aldh adeficiencyaldh amicewhere seizures increase in frequency and severity starting atdays of life to culminate with death at the time of weaningThere is no cure and available treatments are primarily symptomaticIn this proposalwe focus on evaluating the antiseizure properties of farnesol and structurally related analogues in experimental SSADHDFarnesol is a bioactive primary alcohol with neuronal voltage gated Cachannel blocker propertiesactive in alcohol withdrawal seizuresPreliminary work by the research team recently showed that farnesol is a positive allosteric modulator of human GABAA receptors which suppresses seizures in experimental SSADHDThree aims are proposed to further characterize the antiseizure properties of farnesol with an evaluation of dose dependency and long term efficacyAimsandampand to begin to identify the structural determinants of farnesol that are critical to its antiseizure activityAimthis in a phenocopy of the human diseasethe SSADHD knock outaldh amouseThe proposed studies will bridge gaps in the development of targeted therapies for SSADHDwhile providing insight on the use of farnesol and analogues in the treatment of other forms of epilepsies NARRATIVE Inherited succinic semialdehyde dehydrogenase deficiencySSADHDthe most common disorder of GABA metabolismfeatures accumulation ofaminobutyric acidGABAconcomitant down regulation of inhibitory neurotransmission pathwaysand a marked epileptic presentationClassical antiepileptic drugs are used but their efficacy in SSADHD is variable and limited by potential significant side effectshencecalling for identifying new drugs with improved therapeutic efficacyThe novel therapeutic blueprint generated in this proposal will substantively contribute to finding a successful treatment for SSADHD and other disorders of GABA metabolism