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Neuroprotective Apolipoprotein-E Analogs Continuation

Neuroprotective Apolipoprotein-E Analogs Continuation
神经保护性载脂蛋白-E 类似物 延续
批准号:
7683769
负责人:
MICHAEL PETER VITEK
金额:
$105.65万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
已结题
起止时间:
2002-07-15 至 2011-08-31
关键词:
AccountingActivities of Daily LivingAcuteAdverse effectsAdverse eventAmericanAnimal ModelAnimalsAnti-Inflammatory AgentsAnti-inflammatoryApolipoprotein EArea Under CurveBloodBlood Pressure MonitorsBrainBrain Hypoxia-IschemiaCanis familiarisCaringCerebral perfusion pressureCessation of lifeChemistryClassificationClinicalClinical InvestigatorClinical ResearchClinical TrialsComaCongressesContractsDataDependenceDisabled PersonsDocumentationDoseDrug ExposureDrug KineticsEmergency SituationEquilibriumEvaluationExposure toFundingFutureGoalsGrantGuidelinesHalf-LifeHeadHealth care facilityHemorrhageHistopathologyHourHumanHuman IdentificationsHuman VolunteersIndustryInflammationInjuryIntensive CareIntracranial PressureIntravenousInvestigational DrugsInvestigational New Drug ApplicationLabelLeadLearningLifeMarketingMaximum Tolerated DoseMeasuresMemoryMetabolismMethodsMiddle Cerebral Artery OcclusionMissionModelingMonitorMotorMusNeuronal DysfunctionNeuronsOrganOutcomePamphletsPatientsPeptidesPerformancePerinatal HypoxiaPharmaceutical PreparationsPharmacologyPharmacotherapyPhasePhase I Clinical TrialsPhase III Clinical TrialsPhysiologicalPlasmaPoisonPreclinical TestingPreparationProceduresPropertyProtocols documentationPublic HealthQualifyingRattusRecoveryReperfusion InjuryReportingResearch DesignResearch PersonnelRestRodentSafetySaltsSeveritiesShippingShipsSprague-Dawley RatsSteroidsSubarachnoid HemorrhageSupportive careSurvivorsTestingTherapeuticTherapeutic IndexTimeToxic effectToxicity TestsToxicokineticsToxicologyTranslationsTraumatic Brain InjuryUnited StatesUnited States Food and Drug AdministrationUnited States National Institutes of HealthValidationWistar RatsWorkanaloganalytical methodanimal databasebench to bedsideclinically relevantcognitive functioncostdosageefficacy testinggood laboratory practicehuman subjectimmunogenicityimprovedin vivoinjuredintravenous administrationintravenous injectionliquid chromatography mass spectrometrymeetingsmortalitymotor controlmouse modelnovelpre-clinicalpreclinical studypublic health relevanceremediationresearch studyresponseshear stressstandard of caresuccesssynthetic peptidetrait

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中文摘要
翻译
描述(由申请人提供):在我们之前的拨款中,我们已经开发了COG1410,一种具有额外神经保护特性的新型抗炎肽,用于治疗创伤性脑损伤(TBI)。在美国,每年有5万人死于创伤性脑损伤,在接受治疗并从紧急医疗机构出院的100万美国人中,有23万幸存者残疾,他们的余生将需要大量的护理。在开放性和闭合性脑损伤动物模型中,COG1410在损伤后2小时给予。与对照组相比,服用COG1410的动物在平衡、协调、运动控制、学习和记忆测试中的后续表现显著改善。基于动物试验的成功,我们的临床目标是对TBI患者进行药物治疗,以减轻TBI反应的严重程度,从而改善结果,比如能够在没有外界帮助的情况下进行正常和独立的日常生活活动。该申请是为了执行食品和药物管理局(FDA)提交和批准COG1410的研究性新药(IND)申请所需的所有安全性和毒性研究。综上所述,我们需要合成高质量的COG1410,并使用良好实验室规范(GLP)方法分析不同母体下的COG1410,通过静脉注射不同剂量的COG1410测量大鼠和狗的药代动力学(PK)和毒代动力学(TK),评估COG1410在大鼠和狗身上的安全性。此外,还详细说明了IND需要进行的其他研究。该申请的总体目标是成功完成所有研究,提交监管报告并获得必要的批准,以开始COG1410在人体中的1期临床试验。公共卫生相关性:我们开发了COG1410,一种具有额外神经保护特性的新型抗炎肽,用于治疗创伤性脑损伤(TBI)。在美国,每年有5万人死于创伤性脑损伤,在接受治疗并从紧急医疗机构出院的100万美国人中,有23万幸存者残疾,他们的余生将需要大量的护理。目前,FDA还没有批准创伤性脑损伤的治疗方法,此次申请的重点是将COG1410(一种保护动物免受创伤性脑损伤的新药)引入人类临床试验和人类创伤性脑损伤患者。
英文摘要
DESCRIPTION (provided by applicant): In our previous grants, we have developed COG1410, a novel anti-inflammatory peptide with additional neuroprotective properties, for the treatment of Traumatic Brain Injury (TBI). Each year, TBI accounts for 50,000 deaths in the United States and of the 1,000,000 Americans treated and released from the Emergency Health Facilities, 230,000 survivors are disabled to the point that they will require significant care for the rest of their lives. In animal models of open and closed TBI, COG1410 was given 2 hours following the injury. Subsequent performance of COG1410 treated animals was significantly improved compared to controls on tests of balance, coordination, motor control, learning and memory. Based on the success in animals, our clinical goal is to intervene with a drug therapy in TBI patients that would lessen the severity of the response to TBI and thereby improve outcomes, like being capable of normal and independent activities of daily living without external assistance. This application is to perform all of the safety and toxicity studies required by the Food and Drug Administration (FDA) for submission and approval of an Investigational New Drug (IND) application for COG1410. In overview, we are required to synthesize high-quality COG1410 and use Good Laboratory Practices (GLP) methods to analyze COG1410 in different matrices, measure pharmacokinetics (PK) and toxicokinetics (TK) in rats and dogs using different amounts of COG1410 via intravenous injection and assess the safety of COG1410 in rats and dogs. Additional studies required of the IND are also detailed. The overall goal of this application is the successful completion of all studies, regulatory report submissions and necessary approvals that are needed to begin Phase 1 clinical trials of COG1410 in humans. PUBLIC HEALTH RELEVANCE: We have developed COG1410, a novel anti-inflammatory peptide with additional neuroprotective properties, for the treatment of Traumatic Brain Injury (TBI). Each year, TBI accounts for 50,000 deaths in the United States and of the 1,000,000 Americans treated and released from the Emergency Health Facilities, 230,000 survivors are disabled to the point that they will require significant care for the rest of their lives. Currently, there are no FDA approved treatments for Traumatic Brain Injury and the focus of this application is to bring COG1410, an investigational new drug that does protect animals from TBI, to human clinical trials and to human TBI patients.
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DFMO Therapy for Polycystic Kidney Disease
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    10080836
  • 项目类别:
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  • 财政年份:
    2020
  • 负责人:
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  • 项目类别:
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  • 财政年份:
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  • 负责人:
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  • 批准号:
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  • 项目类别:
  • 资助金额:
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  • 财政年份:
    2014
  • 负责人:
    MICHAEL PETER VITEK
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  • 项目类别:
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  • 财政年份:
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  • 负责人:
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  • 依托单位:
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