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Novel pro-drug pharmacotherapy to prevent neuronal and cell degeneration in AMD

Novel pro-drug pharmacotherapy to prevent neuronal and cell degeneration in AMD
预防 AMD 神经元和细胞变性的新型前药药物疗法
批准号:
10216112
负责人:
Peter Koulen
金额:
$5.74万
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-30 至 2022-07-31
关键词:
AcuteAddressAffectAge related macular degenerationAnimal ModelAntioxidantsApoptosisApoptoticAreaBasic ScienceBiologicalBiological ProductsBlindnessCell DeathCellsCharacteristicsChemicalsChoroidal NeovascularizationClinical ResearchComplementCytoprotectionDataDevelopmentDiseaseDisease OutcomeDrug Delivery SystemsDrug DesignDrug KineticsEffectivenessEyeEye diseasesFeasibility StudiesFutureGeneticGoalsHealthHealthcareHumanIn VitroInterdisciplinary StudyInterventionKnowledgeMeasuresMediatingMetabolicMetabolic BiotransformationMethodsMinorityNatureNeuronsNonexudative age-related macular degenerationOral AdministrationOxidative StressPathogenesisPerformancePharmacologyPharmacotherapyPhase I Clinical TrialsPhase II Clinical TrialsPhotoreceptorsPopulationPreclinical TestingPreventionProdrugsPropertyResearchResearch Project GrantsRetinaRetinal DegenerationRetinal PhotoreceptorsRetinal PigmentsRoleRouteSignal PathwayStructureStructure of retinal pigment epitheliumTestingTherapeuticTopical applicationTreatment EfficacyUnited StatesVisionVisualVisual AcuityVisual impairmentVitamin Eage relatedbaseclinical efficacyclinically relevantdesignexperimental studygamma-Tocopherolgene therapyhealth care deliveryhealth disparityhuman modelimprovedin vivoinnovationinsightneovascularizationneuron apoptosisneuron lossneuroprotectionnovelnovel therapeutic interventionnovel therapeuticspreservationpreventretinal damageretinal neuronside effectsmall moleculetherapy designtherapy developmenttreatment strategy

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PROJECT SUMMARY/ABSTRACT Degeneration or acute damage of retinal pigment epithelial (RPE) and nerve cells in the retina due to Age-related Macular Degeneration (AMD) is a major cause of visual loss and blindness in the United States and worldwide. The proposed multidisciplinary research project will focus on the characterization of a novel signaling pathway for and the development of a novel pharmacological intervention to control degeneration of RPE cells and neurons in AMD. To this end, preclinical testing of the new therapeutic strategy will be performed, along with ocular biotransformation, transport and distribution studies, in established models of human AMD. These experiments will determine efficacy of treatment in terminating and/or preventing AMD associated neuronal loss and preservation of visual function, and to generate data to support feasibility for and move positive findings to phase 1 and 2 clinical trials. Specifically, we will test the two-pronged hypothesis that treatment based on the ocular targeting of a novel chemical antioxidant strategy protects RPE cells and neurons from apoptosis by topical delivery in established models of human AMD and, therefore, leads to prevention or improvement of visual impairment and functional deficits associated with AMD. The determination of neuronal viability and the acquired knowledge on associated biopharmaceutical and pharmacological parameters will indicate the potential of the method to remedy AMD as the overall goal of the project. This novel approach for therapy development in AMD focuses on complementary and alternative cellular protection and neuroprotection. The innovative strategy has the potential to generate a first-in-class pharmacotherapy approach for dry AMD using a topical rather than a systemic or invasive route of drug delivery. The strategy’s potentially high impact lies in its capacity to be both preventative and therapeutic in nature and to complement existing treatment designs and rationales addressing other aspects of AMD treatment such as those targeting neovascularization.
期刊论文(4)
专著(0)
科研奖励(0)
会议论文
DOI: 10.3389/fcell.2023.1098406
发表时间: 2023
期刊: Frontiers in cell and developmental biology
影响因子: 5.5
作者: []
通讯作者:
DOI: 10.1186/s12886-022-02585-7
发表时间: 2022-10-20
期刊: BMC OPHTHALMOLOGY
影响因子: 2
作者: [Galindez, Sydney M., Keightley, Andrew, Koulen, Peter]
通讯作者: Koulen, Peter
DOI: 10.3389/fimmu.2023.1138519
发表时间: 2023
期刊: FRONTIERS IN IMMUNOLOGY
影响因子: 7.3
作者: [Duncan, R. Scott, Keightley, Andrew, Lopez, Adam A. A., Hall, Conner W. W., Koulen, Peter]
通讯作者: Koulen, Peter
DOI: 10.3389/fnins.2022.890021
发表时间: 2022
期刊: FRONTIERS IN NEUROSCIENCE
影响因子: 4.3
作者: [Edwards, Genea, Olson, Caroline G., Euritt, Carlyn P., Koulen, Peter]
通讯作者: Koulen, Peter
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