SBIR/STTR Research Award

A novel inhaled dry powder psychoplastogenic formulation for treating persons with opioid use disorder

Award identifier 90294c7b4d73e14c1672f1f2f89b8278360e0044554eb97194a4e9e56b062b26Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$404,917

Program and phase

SBIR · Phase I

Award year

2024

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Quench Medical Inc.
Proposal award date
2024-06-01
Contract end date
2025-05-31
UEI
JVLSL7GNVK25
Solicitation number
PA23-230
Topic code
NIDA

Research abstract

Project Summary Abstract Opioid use disorder (OUD) is characterized by a problematic pattern of opioid use causing significant personal impairment or distress and may lead to overdose and death. In 2021, there were over 2.7 million Americans living with OUD and 106,699 Americans who died from an opioid related overdose. Unfortunately, approved medications to treat OUD carry a high risk of dependence and have had a limited effect. Therefore, new strategies for treating people with OUD should be developed to address the significant unmet need. A new drug class of psychoplastogenic compounds (PC) is being explored for therapeutics promoting structural and functional neural plasticity to treat substance use disorders (SUD). Evidence of anti-addictive effects and pharmacology of PCs have recently been pioneered in the context of psychopathological disorders, including depression, anxiety, and SUD. Single doses of a potent PC, 5-MeO-DMT, have demonstrated long-lasting effects on participants, but little is known about the dosing strategy and potential efficacy of reducing rates and severity of symptoms of patients living with OUD. Inhalation is the primary route of administration of 5-MeO-DMT, but dosing remains uncertain due to means of collection, purification, and inhalation drug delivery. In this case, it seems inhalation is the most efficient systemic delivery mechanism to improve bioavailability and avoid first pass hepatic metabolism but reaching the periphery of the lung for effective systemic delivery is technically challenging. Given the strong need, we propose to create and test in-vivo a highly effective, consistent, and efficiently targeted inhalation treatment using our proprietary dry powder aerosol technology for pulmonary-to-systemic delivery of 5-MeO-DMT. A successful outcome of this project will be the creation and in-vivo efficacy testing of a new type of targeted inhalation formulation containing 5-MeO-DMT to treat OUD. Quench Medical's technology has the potential to have a ground- breaking impact on the field of SUD by delivering 5-MeO-DMT safely, consistently, and effectively to patients living with OUD.

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

7 SBIR/STTR records share this UEI (2018–2025). Reported award amounts total $5,631,185. Reported amounts are not federal obligations.

Phases: Phase I, Phase II, Phase II – Direct to Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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