Automated Molecular Diagnostics for Rapid Detection of Dengue Viremia Using Whole
Automated Molecular Diagnostics for Rapid Detection of Dengue Viremia Using Whole
批准号:
8293163
负责人:
SHUQI CHEN
金额:
$76.51万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2010
资助国家:
美国
项目状态:
已结题
起止时间:
2010-09-01 至 2013-06-30
关键词:
AcuteAlgorithmsAmericanBiological AssayBlood specimenCapitalCenters for Disease Control and Prevention (U.S.)ClinicClinicalClinical ResearchClinics and HospitalsCollaborationsConflict (Psychology)DengueDengue Hemorrhagic FeverDengue VirusDetectionDevelopmentDevicesDiagnosisDiagnosticDiagnostic ProcedureDiagnostic testsDiseaseDistressDoctor of PhilosophyDoseEconomicsEmergency SituationExcisionGrantHeadHealthHepatitis CHospital Information SystemsHospitalsHourHumanHuman ResourcesIn VitroIncidenceInfectionInsect VectorsLaboratoriesLaboratory MarkersLeadLicensingLifeMarketingMexicoMilitary PersonnelMolecularNamesNucleic Acid Amplification TestsNucleic AcidsPatientsPerformancePersonal CommunicationPhasePhysicians&apos OfficesPolymerase Chain ReactionPovertyPreparationProcessPrognostic MarkerQualifyingRNAReadinessReagentReportingResourcesRiskRural HealthSamplingSampling StudiesScanningSensitivity and SpecificitySerotypingServicesSideSmall Business Innovation Research GrantSocial WelfareSystemTechnologyTestingTimeTrainingTranscriptTreatment ProtocolsTubeUnited States National Institutes of HealthViral Hemorrhagic FeversViremiaVirusVirus DiseasesWhole BloodWorld Health Organizationbaseclimate changecommercializationcosthemorrhagic fever virusimprovedinhibitor/antagonistinstrumentmanufacturing processmeetingsnovelnucleic acid detectionoperationpandemic diseasepoint of carepopulation migrationpre-clinicalproduct developmentpublic health relevancerapid detectionrapid diagnosisresearch clinical testingtouchscreenvector
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): We propose to develop a highly sensitive and rapid point-of-care nucleic acid test based on IQuum's lab-in-a-tube (Liat") platform for the diagnosis of patients with dengue fever or dengue hemorrhagic fever from whole blood samples. The Liat Dengue Assay will utilize the Liat Analyzer to enable the minimally trained personnel to perform the dengue infection test at a hospital, clinic or physician's office in less than 1 hour. By enabling effective and sensitive dengue infection testing, we expect that the Liat assay will allow clinicians to quickly diagnose patients with dengue fever or dengue hemorrhagic fever and initiate appropriate treatments. The Liat Dengue Assay overcomes the limitations of current dengue infection tests, whose long turnaround time and technical complexity requires testing to be performed in centralized laboratories, resulting in missed opportunities for disease treatment or the continued use of ineffective treatment regimens. The assay will also be among the first near patient nucleic acid tests, and will provide significant benefit to patient health and welfare, as well as enhance the preparedness for this emerging disease. In Phase I, we propose to transfer the Liat Dengue Assay to manufacturing and perform analytical sensitivity and specificity studies. In Phase II, we propose to complete the analytical studies, develop and validate manufacturing processes for the Liat Dengue Assay, and conduct clinical sample study to validate the assay. At the conclusion of the pre-clinical and analytical studies, we will submit a pre-investigational device exemption (pre-IDE) to the FDA in preparation for expanded clinical study of the Liat Dengue Assay for 510(K) market clearance.
PUBLIC HEALTH RELEVANCE: By enabling effective and sensitive dengue infection testing, the Liat" Dengue Assay will allow clinicians to quickly diagnose patients with dengue fever or dengue hemorrhagic fever. The Liat Dengue Assay overcomes the limitations of current dengue infection tests, whose long turnaround time and technical complexity requires testing to be performed in centralized laboratories, resulting in missed opportunities for disease treatment or the continued use of ineffective treatment regimens. The assay will also be among the first near patient nucleic acid tests, and will provide significant benefit to patient health and welfare, as well as to enhance the preparedness for this emerging disease.
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Automated Molecular Diagnostics for Rapid Detection of Dengue Viremia Using Whole
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批准号:8288382
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项目类别:
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资助金额:$94.2万
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财政年份:2010
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负责人:SHUQI CHEN
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依托单位:
Automated Molecular Diagnostics for Rapid Detection of Dengue Viremia Using Whole
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财政年份:2001
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Lab-in-a Tube Molecular Analyzer
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资助金额:$85.99万
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财政年份:2001
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Lab-in-a Tube Molecular Analyzer
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批准号:6654892
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资助金额:$78.03万
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财政年份:2001
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Lab-in-a-tube test for cytomegalovirus monitoring
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海外基金