Final preclinical development of gene therapy for post-operative atrial fibrillat
Final preclinical development of gene therapy for post-operative atrial fibrillat
批准号:
8635273
负责人:
J Kevin Donahue
金额:
$12.56万
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:
2013-03-15 至 2017-02-28
关键词:
Adenovirus VectorAgeArrhythmiaAtrial FibrillationBiodistributionCardiacCardiac Surgery proceduresCessation of lifeChestClinical TrialsComplicationCongestive Heart FailureDataDevelopmentDiseaseDominant-Negative MutationDoseElderlyEventFamily suidaeFunding OpportunitiesGene DeliveryGene ExpressionGene TransferGenesHeart AtriumHeart DiseasesHospitalsHumanImageryIncidenceIntensive Care UnitsInvestigational New Drug ApplicationLength of StayLifeMethodsModelingMorbidity - disease rateMyocardial InfarctionOperative Surgical ProceduresPatientsPhasePhase I Clinical TrialsPostoperative PeriodPotassium ChannelPreclinical TestingPredispositionPreventionPreventiveProceduresPropertyPublic HealthRefractoryRespiratory FailureRiskSafetyStrokeTestingTherapeuticTimeTissuesToxicologyVentricular Arrhythmiacombatefficacy testingexperienceexpression vectorgene therapymortalitymutantolder patientpre-clinicalpreventpublic health relevanceresponserisk variantvector
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Post-operative atrial fibrillation (POAF) is the most common complication following cardiac surgery. POAF increases morbidity and mortality after surgery, increases length of stay in the ICU and hospital, and increases risks of stroke, congestive heart failure, myocardial infarction and death. The impact on public health is substantial. In particular, POAF is a problem of the elderly, because the need for cardiac surgery, and the incidence, morbidity and mortality of POAF all increase as a function of age. Currently available preventative strategies still allow a 30% incidence of POAF. To combat this problem, we propose gene therapy as a new strategy to prevent POAF. We have efficacy and safety data in a pig model of POAF that shows prevention of sustained AF for 2 weeks after atrial gene painting of AdKCNH2-G628S, a time that coincides with the window of risk for POAF. We saw no proarrhythmia or other negative effects after atrial gene painting. Here, we propose formal preclinical testing of AdKCNH2-G628S with the following specific aims: (1) to successfully complete a dose-ranging study that defines minimum effective dose, and (2) to successfully complete a formal preclinical biodistribution and toxicology testing that defines maximum safe dose. Successful completion of these aims will complete the necessary preclinical testing before moving this potential life-saving therapy to clinical trial.
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依托单位:
GENE TRANSFER APPROACHES TO ATRIAL FIBRILATION
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资助金额:$39.25万
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依托单位:
GENE TRANSFER APPROACHES TO ATRIAL FIBRILATION
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GENE TRANSFER APPROACHES TO ATRIAL FIBRILATION
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依托单位:
GENE TRANSFER APPROACHES TO ATRIAL FIBRILATION
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资助金额:$39.25万
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Improved Methods for Myocardial Gene Transfer
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负责人:J Kevin Donahue
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依托单位:
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