课题基金 / 基金详情

Glomerular Filtration Rate Test

Glomerular Filtration Rate Test
肾小球滤过率测试
批准号:
7263670
负责人:
CHRISTOPHER P REINHARDT
金额:
$7.75万
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:
2007-09-15 至 2008-08-31
关键词:
AdultAffectAffinityAffinity ChromatographyAmericanAnimal ExperimentationAntibodiesAntibody FormationBiochemicalBiological AssayBiological MarkersBloodCarrier ProteinsChronic Kidney FailureClassClinicalClinical Practice GuidelineClinical ResearchConditionCreatinineDataDevelopmentDiagnosisDiagnosticDiagnostic ProcedureDiagnostic testsDiet ModificationDietary InterventionDiseaseEarly DiagnosisEffective Renal Plasma FlowEnd stage renal failureEnzyme-Linked Immunosorbent AssayEpidemicEquationFiltrationFoundationsFundingGadolinium DTPAGadopentetate DimeglumineGlomerular Filtration RateGoalsGoldHaptensHealth Care CostsHumanImaging TechniquesImmune SeraImmune responseImmunoassayInjection of therapeutic agentInulinKidneyKidney DiseasesKineticsLegal patentMagnetic Resonance ImagingMarketingMeasurementMeasuresMedicalMetabolic Clearance RateMethodsMolecular WeightMonitorMorbidity - disease rateNumbersOrganOryctolagus cuniculusOutcomePatientsPerformancePharmacologic SubstancePhasePopulationPrincipal InvestigatorProceduresProcessProductionPublishingRadioactiveRangeReagentRenal clearance functionRenal functionResearchResearch PersonnelRiskSerumSmall Business Funding MechanismsSmall Business Innovation Research GrantStagingStandards of Weights and MeasuresSystemTechniquesTechnologyTestingTimeUnited StatesUnited States Food and Drug AdministrationUrineWorkbaseclinical applicationcostcross reactivitydesignhealthy volunteerimmunogenicimprovedin vivointerestmonoclonal antibody productionmortalitynovelpolyclonal antibodypost gamma-globulinsprogramsresponsesize

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中文摘要
翻译
描述(申请人提供):肾脏疾病在美国被描述为一种流行病。超过2000万患者患有慢性肾脏疾病(CKD),而且这个数字每年都在增加。因此,预计在1999至2010年间,终末期肾病(ESRD)患者的数量将翻一番。CKD和ESRD的这些增加与显著的发病率、死亡率和医疗费用相关。肾脏疾病的早期发现和治疗已被证明可以改善预后,但肾脏疾病往往被低估,导致失去治疗机会。肾脏疾病早期诊断和治疗的重要性已经被广泛审查,并被国家肾脏基金会作为K/DOQI临床实践指南出版。监测肾小球滤过率(GFR)的变化为早期发现肾脏疾病提供了最佳手段。在美国,用来筛查肾小球滤过率异常的最广泛的检测方法是血清肌酐。然而,与使用理想的滤过性标记物(如菊粉)直接测量GFR的方法相比,使用血清肌酐估计的GFR值的诊断价值有限。这一第一阶段的应用寻求支持,以进一步开发一种基于免疫分析技术的新型读出系统,以直接测量GFR。我们建议的测试将是准确的、简单易用的、廉价的,并将被广泛评估。这项测试将使用FDA批准的已知为GFR标志物的化合物。因此,我们建议的GFR测试将能够更快地进入市场。该项目将进一步开发一种诊断测试来测量肾功能。这项测试将利用众所周知和广泛可用的分析技术,并将利用临床上可用的化合物。因此,这一测试将能够迅速进入市场。
英文摘要
DESCRIPTION (provided by applicant): Kidney disease in the United States has been described as an epidemic. More than 20 million patients have chronic kidney disease (CKD) and these numbers are increasing annually. As a result, the number of patients with end-stage renal disease (ESRD) is expected to double between 1999 and 2010. These increases in CKD and ESRD are associated with significant morbidity, mortality and healthcare costs. Early detection and treatment of kidney disease has been shown to improve outcomes, but kidney disease is often under diagnosed resulting in lost opportunities to treat. The importance of early diagnosis and treatment of kidney disease has been extensively reviewed and published as a K/DOQI clinical practice guideline by the National Kidney Foundation. Monitoring changes in glomerular filtration rate (GFR) provides the best means for early detection of kidney disease. The test that is most widely used in the US to screen abnormalities in GFR is serum creatinine. However, estimated GFR values using serum creatinine have limited diagnostic value over methods that directly measured GFR using an ideal filtration marker, such as inulin. This Phase I application seeks support to further develop a novel readout system, based on immunoassay technology, to directly measure GFR. Our proposed test will be accurate, simple-to-use, inexpensive and will be widely assessable. The test will utilize FDA-cleared compounds that are known to be GFR markers. As a result, our proposed GFR test will be able to more quickly enter the marketplace. The project will further develop a diagnostic test to measure kidney function. The test will utilize well-known and widely available analytical technology and will utilize clinically available compounds. Therefore, this test will be able to quickly enter the market-place.
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