SBIR/STTR Research Award

Preclinical Development of Novel MEK1/2 Inhibitors to Treat Inherited Cardiomyopa

Award identifier 10fe1d500b5edd0acfb717fadd42b92b9edcd7ceb0d025e63f90f1a546c8da37Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$99,976

Program and phase

STTR · Phase I

Award year

2013

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
CHEMINPHARMA, LLC
Proposal award date
Not reported
Contract end date
Not reported
UEI
Not reported
Solicitation number
PA12-089
Topic code
NCATS

Research abstract

DESCRIPTION (provided by applicant): Cardiomyopathy is an anatomic and pathologic condition associated with muscle and electrical dysfunction of the heart, usually with inappropriate ventricular hypertrophy or dilatation. There are various causes of cardiomyopathy, many of which are genetic. Dilated cardiomyopathy, the most common form, is characterized by an increase in both myocardial mass and volume. There is no definitive, curative treatment. Research performed at Columbia University has revealed that abnormal activation of the extracellular signal-regulated 1/2 (ERK1/2) branch of the mitogen-activated protein kinase (MAPK) cascade occurs in hearts of Lmna H222P knock-in mice, a model of inherited dilated cardiomyopathy caused by mutation in the lamin A/C gene, which is responsible for about 8% of inherited dilated cardiomyopathies in humans. The research at Columbia has further shown that inhibitors of MAPK/ERK kinase1/2 (MEK1/2), the enzyme that activates ERK1/2, prevent ventricular dilatation, improvecardiac contractility and delay the development of fibrosis in Lmna H222P mice. The goal of the present Small Business Technology Transfer grant proposal is to develop and commercialize this discovery made at Columbia into a treatment for human patients with cardiomyopathy caused by lamin A/C gene mutation. The project is a collaborative effort between Cheminpharma LLC, which has invented and synthesized a proprietary and potent MEK1/2 inhibitor, and the scientists at Columbia who made the initial discoveries. Aim 1 is to test Cheminpharma's novel MEK1/2 inhibitor, CIP-137401, in the Lmna H222P mouse model of dilated cardiomyopathy. Aim 2 is to carry out a synthetic route of CIP-137401 to allow for the efficient synthesis of material to support IND enablingstudies. This proposal will identif a proprietary MEK1/2 inhibitor with in vivo activity that could be suitable for clinical developmen to treat patients with inherited dilated cardiomyopathy. PUBLIC HEALTH RELEVANCE PUBLIC HEALTH RELEVANCE: Cardiomyopathy is a life-threatening disease that leads to heart failure and death for which there is currently no curative treatment. This project is designed to develop and commercialize a novel drug known as a MEK1/2 inhibitor to treat cardiomyopathy, initially focusing on a specific inherited type.

Technology keywords

Not reported

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Agency intelligence

Department of Health and Human Services

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