Aldosterone Synthase Inhibitor for CKD
Aldosterone Synthase Inhibitor for CKD
批准号:
8453692
负责人:
Bert J. W. M. Oehlen
金额:
$38.09万
依托单位国家:
美国
项目类别:
财政年份:
2013
资助国家:
美国
项目状态:
已结题
起止时间:
2013-06-20 至 2014-05-31
关键词:
AlbuminuriaAldosteroneAldosterone SynthaseAngiotensin ReceptorAngiotensin-Converting Enzyme InhibitorsAnimal ModelApplications GrantsAromataseBenchmarkingBlood PressureCYP11B1 geneCYP11B2 geneCYP19A1 geneCYP3A4 geneCellsChemistryChronic Kidney FailureClinical ManagementCollagenCreatinineCreatinine clearance measurementCytochrome P450DepositionDevelopmentDiabetic NephropathyDiseaseDoseDrug ExposureDrug KineticsEnzyme InhibitionEnzymesFibrosisFunctional disorderFutureGoalsHistopathologyHomology ModelingHydroxyprolineKidneyKidney DiseasesLeadLibrariesMeasurementMineralocorticoid ReceptorModelingMusNephrectomyObstructionOralPeptidyl-Dipeptidase APharmaceutical PreparationsPharmacodynamicsPharmacologyPhasePhysiologicalPhysiologyPlayPre-Clinical ModelProductionPropertyPublishingRattusRenin-Angiotensin-Aldosterone SystemRodent ModelRoleSafetySeriesSerumSolidSpironolactoneSystemTestingTherapeuticToxicologyTreatment EfficacyUrethral ObstructionUrineWorkbaseclinically relevantclinically significantcombatdrug efficacyefficacy evaluationefficacy testinginhibitor/antagonistpre-clinicalpreventpublic health relevanceresearch clinical testingsmall moleculesuccesstelmisartantherapeutic effectivenesstool
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): The renin-angiotensin-aldosterone system (RAAS) plays a critical role in renal physiology. Inhibitors of angiotensin-converting enzyme (ACE) or angiotensin receptor blockers (ARB) are the mainstay in the clinical management of renal disorders such as chronic kidney disease (CKD). These treatments are thought to work in large part by reducing serum and renal aldosterone levels. However, despite initial success of ACE inhibition or ARB therapy to reduce aldosterone, levels eventually often return to pretreatment levels, thus limiting therapeutic effectiveness of RAAS inhibitors. The clinical significance of th phenomenon of "aldosterone breakthrough" is increasingly recognized. One approach to combat this breakthrough is to inhibit the enzyme responsible for aldosterone production: aldosterone synthase. Despite promising results of tool aldosterone synthase inhibitors in preclinical animal models, no aldosterone synthase inhibitors are currently undergoing clinical evaluation for CKD. From a focused library, Angion has identified a new series of proprietary non- steroidal small molecule inhibitors of aldosterone synthase. The present grant proposal aims to (1) optimize this series of compounds and (2) test efficacy in preclinical models of renal fibrosis.
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