Carboxyamidotriazole for Neovascular Ocular Disease
Carboxyamidotriazole for Neovascular Ocular Disease
批准号:
7277088
负责人:
Maria Bartolomeo Grant
金额:
$15.2万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2007
资助国家:
美国
项目状态:
已结题
起止时间:
2007-09-30 至 2008-08-31
关键词:
AffectAge related macular degenerationAgingAngiogenesis InhibitorsAnimal ModelBiological AssayCalciumCarboxyamidotriazoleChoroidal NeovascularizationCombined Modality TherapyCompatibleDevelopmentDiseaseDoseDrug FormulationsEndothelial CellsEtiologyGrantGrowth FactorHealth Care CostsHumanIn VitroInvasiveMalignant NeoplasmsMediatingModelingMolecularMusOralOxygenPatientsPermeabilityPharmaceutical PreparationsPharmacologyPharmacotherapyPhasePhase II Clinical TrialsPopulationProcessResearch PersonnelRetinalRetinal DiseasesRetinopathy of PrematurityRoleRouteSafetySystemic TherapyTestingTherapeuticUnited States Food and Drug AdministrationVascular Endothelial Growth Factorsage groupangiogenesisbasebevacizumabcancer therapyclinical efficacycostcost effectivedesirediabeticimprovedinhibitor/antagonistmouse modelneovascularnovelocular neovascularizationpreclinical studyproliferative diabetic retinopathysmall molecule
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Neovascular ocular diseases as exemplified by retinopathy of prematurity (ROP), proliferative diabetic retinopathy (PDR) and "wet" age-related macular degeneration (AMD) are severe diseases affecting all age groups in the US. Recently, there has been progress in neovascular ocular disease drug therapy based on large molecule VEGF inhibitors. Nevertheless, novel drug therapies are needed that i. have new mechanisms of action ii. are highly efficacious iii. are amenable to less invasive ocular administration and iv. are highly cost effective. We believe that this need will best be met with classical small molecule synthetic organic drugs that can be manufactured at low cost and have high transcleral permeability. This proposal centers on just such a small molecule anti- angiogenic compound, carboxyamidotriazole (CAI). CAI has a novel mechanism of action, demonstrated efficacy in mouse ocular neovascularization models and has transcleral permeability. Herein, we aim study the potential of CAI to treat neovascular disease by ocular delivery. To this end in Phase I we will i. develop ocular formulations of carboxyamidotriazole (CAI) ii. test the anti-angiogenic effects of CAI in human retinal endothelial cells and iii. test the intravitreal ocular efficacy and safety of optimal CAI formulation(s) in the OIR model and choroidal neovascularization (CNV) models. Novel drug therapies are needed that have new mechanisms of action are highly efficacious and amenable to less invasive ocular administration while being highly cost effective. We believe that this need will best be met with classical small molecule synthetic organic drugs that can be manufactured at low cost and have high transcleral permeability.
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专著(0)
科研奖励(0)
会议论文
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海外基金