SBIR/STTR Research Award
Development and Commercialization of Predictive Biomarker Panel and In Office Kit for the Management of Diabetic Macular Edema
Award amount
$219,009Program and phase
SBIR · Phase IAward year
2017Award 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