SBIR/STTR Research Award

Development of novel pharmacotherapies for AUD

Award identifier 60e7e1b6aa1eb51d7e6ce07f01b2565383a7ec0fb0aed2b010c5a24a68b540eaAwarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$392,942

Program and phase

STTR · Phase I

Award year

2022

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
NEUROEPIGENIX, LLC
Proposal award date
2022-03-01
Contract end date
2023-02-28
UEI
GEWFVH8MVAH4
Solicitation number
PA20-265
Topic code
150

Research abstract

Project Summary The overall goal of this proposal is to characterize a lead compound with a novel mode of action (MOA) that reduces both stress- and dependence-related alcohol drinking in a preclinical model of Alcohol Use Disorder (AUD). AUD is a major problem in the U.S. as approximately 13.9% of adults meet AUD criteria per year. The annual economic burden of AUD is estimated at andgt;$200 billion and AUD is a leading cause of preventable deaths in the USA. Persistent alcohol abuse and dependence is difficult to treat in part because alcohol increases the reactivity of the body’s stress systems. The influence of stress systems facilitates the “the dark side of addiction”, and stress is a primary factor that triggers relapse. Therefore, pharmacotherapies that can reduce stress- and dependence-associated alcohol drinking could reduce both heavy drinking and stress-triggered relapse in individuals suffering from AUD. We recently discovered that systemic administration of an epigenetic enzyme inhibitor reduced both stress- and dependence-potentiated alcohol drinking in a preclinical model. We have filed for patent protection of this entirely novel MOA to treat AUD, which provides a commercial path forward. In this Phase I STTR application, we will evaluate oral bioavailability of our lead compound to examine whether the preferred oral method of delivery is feasible for AUD treatment. We will also examine maximum tolerated dose (MTD) and behavioral toxicity measures. We will then determine optimal dosing conditions, and we seek to establish strong proof-of-principle data that these compounds reduce dependence- and stress-related alcohol drinking in multiple preclinical models and multiple mouse strains in both male and female mice. At the conclusion of these aims, we expect to have sufficient pre-clinical information for subsequent Phase II STTR studies targeting a future Investigational New Drug (IND) application.Project Narrative We have identified a lead compound with a novel mode of action that is capable of reducing both stress- and dependence-related alcohol drinking in a preclinical model of alcohol use disorder (AUD). NeuroEpigenix will extend these initial studies to further develop the lead compound for potential treatment of AUD.

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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