SBIR/STTR Research Award

Farnesol as Novel Treatment in Succinic Semialdehyde Dehydrogenase Deficiency (SSADHD)

Award identifier 6244ffb26f42a8f634c19ca09c0432a048b9761f6afaa43dfba85e23b638b4a4Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$223,095

Program and phase

STTR · Phase I

Award year

2018

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
SPERAGEN, INC.
Proposal award date
2018-08-01
Contract end date
2019-07-31
UEI
QNDHFYNXUNV5
Solicitation number
PA17-303
Topic code
102

Research abstract

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

Technology keywords

Not reported

Other awards by this recipient

Verified by the same UEI. These are other public SBIR/STTR award pages, not a merged company record.

Awards with the same topic code

Verified by an exact topic code match. This is not a text-similarity match.

Research funding history

3 SBIR/STTR records share this UEI (2016–2018). Reported award amounts total $671,069. Reported amounts are not federal obligations.

Phases: Phase I

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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