SBIR/STTR Research Award

Novel ClopNPT for the treatment of acute coronary syndrome

Award identifier 0ba70b12582d3ab0f9e69b6b7ac09e44e3a7f747d459cb7e91385401d18a3468Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$225,000

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
Diapin Therapeutics LLC
Proposal award date
2017-08-01
Contract end date
2018-03-31
UEI
GSWNHA3JGZ93
Solicitation number
PA16-302
Topic code
NHLBI

Research abstract

ABSTRACT Diapin Therapeutics LLC is a preclinical stage company committed to develop new antiplatelet agents for the treatment of acute coronary syndrome associated with diabetes patients Patients with diabetes exhibit platelet hyper reactivity and are at increased risks of adverse cardiovascular events Clopidogrel is the most broadly used P Y inhibitor to prevent arterial thrombosis However clopidogrel has manifested clinical limitations of interindividual variability delayed onset of action and drug drug interactions These limitations are exacerbated in diabetes patients leading to elevated risks of ischemic complications Although newer P Y inhibitors such as prasugrel and ticagrelor have been shown to have better platelet inhibition the risk of bleeding of these inhibitors is still significantly higher than that of clopidogrel therapy Due to the epidemic growth of diabetes in the United States the number of diabetes patients receiving antiplatelet therapy is projected to increase significantly in the next decade Therefore there is a critical need to develop antiplatelet agents with improved benefit risk ratio for diabetes patients We have licensed exclusively an intellectual property from University of Michigan to develop ClopNPT a novel conjugate of clopidogrel Preliminary studies in animal models have shown that ClopNPT rapidly andlt min release the active metabolite AM of clopidogrel with high exposure effectively preventing formation of occlusive arterial thrombi ClopNPT at the effective dose to inhibit occlusive thrombi does not increase bleeding Release of the AM from ClopNPT requires glutathione GSH only and not CYP enzyme that is the main contributor to the clinical limitations of clopidogrel Based on these data we hypothesize that development of ClopNPT that has eliminated the clinical limitations of clopidogrel is an effective strategy to optimize the benefit risk ratios for antiplatelet therapy in patients with diabetes The aim of this proposal is to evaluate clinical risk of ClopNPT by comparing the efficacy and safety with those of clopidogrel ticagrelor and prasugrel in a rabbit arterial model of thrombosis We will determine the time to occlusion following ferric chloride induced vascular injury as well as tongue bleeding time This study will provide significant information whether ClopNPT is able to reduce the risks of bleeding which allows us to conduct preclinical studies required for application of Investigational New Drug Project Narrative Coronary heart disease is one of the leading causes of death in the United States There is a growing demand for more efficacious and safer antiplatelet agents to prevent thrombosis in patients with acute coronary syndromes The proposed study is expected to accelerate the development of novel antiplatelet agents that will improve survival and prognosis of diabetes patients with acute coronary syndromes

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 (2015–2017). Reported award amounts total $2,706,664. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services

Agency intelligence

Department of Health and Human Services

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