SBIR/STTR Research Award

Inhalational A Apolipoprotein A Mimetic Peptide for the Treatment of Asthma

Award identifier 83bbd4c0686d2dc52942434830cd7da418ebf4201cbf8a7f10baf6c84f1b3507Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$293,218

Program and phase

SBIR · Phase I

Award year

2017

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
Technology Holding, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
U52NGYKN42H6
Solicitation number
Not reported
Topic code
NHLBI

Research abstract

SummaryNew treatments are needed for severe asthmatics who do not respond to standard therapy with inhaled steroids especially those with a type low phenotype such as individuals with neutrophil predominant inflammation This solicitation is for the development and early commercialization of an inhalational formulation of the A apolipoprotein A I apoA I mimetic peptide that can be administered to asthmatic subjects in Phase I clinical trials and subsequently developed into a new treatment for severe asthma ApoA I is the major protein component of high density lipoproteins which mediates reverse cholesterol transport out of cells by interacting with the ATP binding cassette subfamily member ABCA ApoA I also has anti inflammatory anti oxidant and immunomodulatory properties NHLBI investigators have shown that systemic administration of the A apoA I mimetic peptide which is a bi helical peptide that recapitulates the helical structure of apoA I and mediates reverse cholesterol transport out of cells by interacting with ABCA attenuates the induction of airway inflammation mucous cell metaplasia and airway hyperresponsiveness in house dust mite HDM challenged mice In addition they have shown that apoA I has a protective effect in allergic asthma Apoa knockout mice which were sensitized and challenged with ovalbumin OVA have increased neutrophilic airway inflammation that was primarily mediated by increased G CSF expression with associated increases in type IFN TNF and Th IL A cytokines The increased neutrophilic airway inflammation in the OVA challenged Apoa knockout mice was inhibited by intranasal administration of the A apoA I mimetic peptide Lastly serum apoA I levels are positively correlated with FEV in atopic asthmatic subjects which suggests that circulating apoA I may improve airflow obstruction These murine and human translational studies serve as the conceptual basis for developing the A apoA I mimetic peptide into a novel inhalational treatment for severe asthma Project GoalsThe overall goal of this project is to prepare in both manufacturing processes and preclinical evaluation an inhalational A apoA I mimetic peptide that will be the subject of a future Investigational New Drug IND application to the US Food and Drug Administration FDA focused on the treatment of type low phenotype asthma patients such as those with neutrophil predominant inflammation Successful submission and allowance to proceed of the IND will enable the company to collaborate on the conduct of a clinical trial with intramural clinicians at the NIH Clinical Center at the company s discretion During review preference will be given to companies or teams with a demonstrated prior ability to successfully bring either a peptide therapeutic or an inhalational therapeutic to at a minimum Phase clinical studies in the US

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

138 SBIR/STTR records share this UEI (1983–2025). Reported award amounts total $44,688,257. Reported amounts are not federal obligations.

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

Agencies: Department of Defense, Department of Energy, National Science Foundation, National Aeronautics and Space Administration, Environmental Protection Agency, Department of Agriculture

Agency intelligence

Department of Health and Human Services

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