SBIR/STTR Research Award

Development and Commercialization of Predictive Biomarker Panel and In Office Kit for the Management of Diabetic Macular Edema

Award identifier 8ba3faa457c20b231e01a4672214ccefc29b4679da988f0cc50ec76abe23c982Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$219,009

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
OCULAR PROTEOMICS, LLC
Proposal award date
2017-09-30
Contract end date
2019-09-29
UEI
Not reported
Solicitation number
PA16-302
Topic code
N

Research abstract

Abstract Diabetic Macular Edema DME is a vision threatening stage in Diabetic Retinopathy DR that can result in legal blindness The biochemical mechanisms that drive DME progression are not well understood and treatments address only portions of the disease pathology The available treatment options vary widely from injectable anti VEGF to injectable steroids to laser treatments and carry a heavy cost burden to the US at over $ million per year Currently there are two large problems with the available treatment options the efficacy of each treatment is highly variable from patient to patient and sustained responses are unpredictable Given the significant increase in diagnoses and the enormous public cost burden there is a need to develop novel functional biomarker diagnostics which assist physicians in choosing the most effective therapy for each patient We are developing a companion diagnostic assay for DME which can be used in a clinic setting to allow physicians to predict outcome to anti VEGF treatment the first line of therapy for DME This assay will enable personalized therapy for each DME patient by determining appropriate therapy before DME treatment is started when to switch treatments and when treatment can be safely stopped which is currently not possible Furthermore as the assay is composed of biomarkers specifically for DME it can be utilized by pharmaceutical companies for discovery development and testing of novel or repurposed drugs for DME We hypothesize that proteomic analysis of relevant pathways in the vitreous proteome and correlation with clinical symptoms of DME patients receiving anti VEGF treatment will enable us to develop a predictive biomarker panel for anti VEGF response in DME We will use Reverse Phase Protein Microarray assay to detect proteins in vitreous samples collected from DME patients receiving anti VEGF treatment over time Targets to be tested include proteins associated with angiogenesis proliferation inflammation immune response ischemia hypoxia and apoptosis cell survival Statistical analysis will be performed to examine whether vitreous protein levels are correlated to changes in retinal thickness and visual acuity in response to monthly anti VEGF treatment The following specific aims are designed to test our hypothesis and to identify a biomarker panel that predicts treatment response Identify biochemical pathways involved in changes in retinal thickness and visual acuity in response to anti VEGF treatment and Identify a panel of biomarkers that is predictive of changes in retinal thickness and visual acuity in response to anti VEGF treatment Successful completion of this project will lead to the development of a predictive biomarker panel in the form of a companion diagnostic kit that assists clinicians in determining the most effective therapy for each DME patient Furthermore our findings will allow us to collaborate with pharma companies in development of new drug targets NARRATIVE Ocular Proteomics LLC is dedicated to improving the vision of patients with various ocular diseases The proposed research project will contribute to public health by identifying a biomarker panel that assists clinicians in determining the most effective therapy for each patient with diabetic macular edema This project will ultimately lead to the development of an assay device that can be used in medical offices

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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