SBIR/STTR Research Award

Targeting PDGFs for Potential Treatment of Proliferative Vitreoretinopathy

Award identifier 76ecb5c321a341c2e43beac57267944cead213593ed51d559fef55e7c35fdcd6Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$224,946

Program and phase

SBIR · Phase I

Award year

2019

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
APTITUDE MEDICAL SYSTEMS INC
Proposal award date
2019-09-30
Contract end date
2020-09-29
UEI
NWWEFYLD9JC3
Solicitation number
PA18-574
Topic code
NEI

Research abstract

Abstract SignificanceProliferative vitreoretinopathyPVRis a blinding orphan indication that occurs inof patients receiving rhegmatogenous retinal reattachment surgeryand accounts forof all primary surgical failuresPVR is characterized by migration and proliferation of ectopic cells beneath or on the surface of the retinawhich then assemble into a membranecausing retinal traction and detachmentSince currently there is no effective therapeutics that reverse the cell proliferation processthe only treatment option for PVR is additional surgerieswhich often have very poor vision outcome due to retinal damage from recurrent detachmentrisking blindnessThere is an urgent unmet need for novel pharmacotherapies for PVRHypothesis and aimsExtensive research established PDGFs as leading candidates for treating PVRHoweverinhibiting multiple PDGF targets may be required to be effectiveAptamers are single stranded oligonucleotides that bind to molecular targets in a similar manner to monoclonal antibodiesmAbsbut possess unique advantages for treating ocular diseases such as PVRthanks to its small sizesuperior stabilityand lack of immunogenicityWe have already developed a fully modified aptamer for PDGF Band verified its potency and stability in vitro and bioactivity in vivo in two different animal modelsWe propose to developmodifiedhigh potency aptamers against PDGF ABandCto extend the key advantages of aptamers to this potential first in class treatment NarrativeProliferative vitreoretinopathyPVRis a blinding orphan indication that occurs inof patients receiving rhegmatogenous retinal reattachment surgeryand accounts forof all primary surgical failuresPVR is characterized by migration and proliferation of ectopic cells beneath or on the surface of the retinawhich then assemble into a membranecausing retinal traction and detachmentSince currently there is no effective therapeutics that reverse the cell proliferation processthe only treatment option for PVR is additional surgerieswhich often have very poor vision outcome due to retinal damage from recurrent detachmentrisking blindnessWe aim to develop next generation aptamers that effectively inhibit cell proliferation and membrane formationand serve as a potential first in class pharmacotherapy for PVR

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

24 SBIR/STTR records share this UEI (2014–2022). Reported award amounts total $15,162,025. Reported amounts are not federal obligations.

Phases: Phase I, Phase II

Agencies: Department of Health and Human Services, Department of Defense

Agency intelligence

Department of Health and Human Services

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