Targeting tau for the development of novel Alzheimer's disease therapeutics
Targeting tau for the development of novel Alzheimer's disease therapeutics
批准号:
10010108
负责人:
Glenn Larsen
金额:
$147.6万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-15 至 2022-04-30
关键词:
Alzheimer&aposs DiseaseAlzheimer&aposs disease brainAlzheimer&aposs disease modelAlzheimer&aposs disease patientAlzheimer&aposs disease therapeuticAlzheimer&aposs disease therapyAnimal ModelBehavioralBiologicalBiological AssayBiologyBostonCanis familiarisCellsChemicalsChronic stressClinicComplexDepositionDevelopmentDiseaseDisease ManagementDisease ProgressionEnvironmentFunctional disorderGenetic PolymorphismGrantHumanImpaired cognitionIndustry StandardLaboratoriesLaboratory ResearchLeadLinkLiquid substanceMembraneMemory LossMessenger RNAMolecular TargetMusMutationNerve DegenerationNeurodegenerative DisordersNeurofibrillary TanglesNeuronsOralPathologicPathologyPathway interactionsPharmaceutical ChemistryPharmaceutical PreparationsPharmacologic SubstancePhaseProcessProteinsRattusRoleSamplingSenile PlaquesSenile dementiaSeriesSmall Business Innovation Research GrantSocietiesSourceStressStructureSynapsesTauopathiesTestingToxicologyTransgenesTranslatingUniversitiesabeta accumulationadvanced diseaseanalogcerebral atrophycholinergic neuroncognitive functiondesigndrug candidatedrug developmenteffective therapyefficacy testinghigh throughput screeningimprovedin vivoinhibitor/antagonistknock-downlead optimizationmedication safetymouse modelneuron lossnew therapeutic targetnovelnovel therapeutic interventionpharmacophorephase 1 studyprogramsproteostasisresponsesafety assessmentsafety studyscreeningsmall moleculesmall molecule inhibitorstemstress granulestress reductionsymptomatic improvementtargeted treatmenttau Proteinstau aggregationtau interactiontherapeutic development
中文摘要
项目总结
英文摘要
PROJECT SUMMARY
Alzheimer’s Disease is a neurodegenerative disease characterized by a progressive decline in cognitive
function and a corresponding accumulation of β-amyloid plaques and neurofibrillary tangles, the two hallmark
pathologies. Drugs currently available to AD patients manage the disease symptoms by improving neuronal
activity, but efficacy diminishes as the disease advances. In tauopathies such as AD, the accumulation of tau
correlates closely with neuronal loss and decline of cognitive function. The novel targeted approach to AD drug
development proposed by Aquinnah Pharmaceuticals stems from discoveries made by Dr. Ben Wolozin
(Boston University and co-founder of Aquinnah) and his laboratory, in which tau pathology (in both AD brain
samples and animal models) was observed in stress granules (SG). Aquinnah is advancing these compelling
findings to further the development of novel molecules that inhibit the formation of tau-SGs as a novel
treatment for AD that were identified in SBIR Phase I. The overall objective of this SBIR Phase II application is
to perform a medicinal chemistry hit-to-lead and lead optimization program to advance our novel compounds
for the treatment of AD.
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