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Multisite Controlled Trial of Cocaine Vaccine (1of 6) Lead Site/ Houston Treatmen

Multisite Controlled Trial of Cocaine Vaccine (1of 6) Lead Site/ Houston Treatmen
可卡因疫苗多中心对照试验(6 中之一)牵头中心/Houston Treatmen
批准号:
7513380
负责人:
THOMAS Richard KOSTEN
金额:
$47.81万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2008
资助国家:
美国
项目状态:
已结题
起止时间:
2008-09-15 至 2013-01-31
关键词:
AIDS pharmacotherapyAbstinenceAcquired Immunodeficiency SyndromeAcuteAddressAdministrative CoordinationAdverse effectsAll SitesAntibodiesAntibody FormationAntigen-Antibody ComplexAttenuatedAuthorshipBackBindingBiological AssayBlood - brain barrier anatomyBlood CirculationBrainCensusesCholera Toxin Protomer BClinical TrialsCocaineCocaine AbuseCognitive TherapyCommunicationComplementConnecticutCoupledDailyDataData AnalysesDoseDropoutDrug AddictionDrug abuseDrug usageEducational process of instructingElectronic MailElectronicsEvaluationExposure toHumanIllicit DrugsImmunologyIndividualIndustryInjection of therapeutic agentJointsLaboratoriesLeadLettersManualsManufacturer NameMeasuresMedicalMedicineMental DepressionMethamphetamineMonitorNational Institute of Drug AbuseNew YorkNucleus AccumbensNumbersOutcomeOutpatientsPaperPatient Self-ReportPatientsPennsylvaniaPharmaceutical PreparationsPharmacistsPharmacologic SubstancePharmacotherapyPilot ProjectsPlacebo ControlPlacebosPopulationProceduresProcessPublic HealthPublicationsQualifyingRandomizedRandomized Clinical TrialsRangeRateRecombinantsRecruitment ActivityRelapseReportingResearchResearch PersonnelRiskRouteSafetySample SizeSamplingScheduleSiteSmokeSmokingStatistical Data InterpretationStructureStudy SectionTelephoneTestingTherapeuticTimeTimeLineToxicologyTrainingTreatment ProtocolsUnited States Food and Drug AdministrationUniversitiesUpdateUrineVaccinationVaccinesVariantWeekWithdrawalWorkWritingaddictionbasebenzoylecgoninecollegecontingency managementcopingcostcravingdata managementdaydesigndrug cravingexperiencefollow-upimmunogenicityinnovationintravenous administrationnovel strategiesnovel vaccinesplacebo controlled studypreventprogramsrandomized placebo controlled trialrapid techniqueresponsesizeskillssuccesssymposiumvaccine effectivenessvaccine efficacy

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DESCRIPTION (provided by applicant): This 16 week, six site, placebo-controlled randomized, clinical trial (PC-RCT) among 300 cocaine dependent patients is designed to test the efficacy of a newly developed active vaccine against cocaine (TA-CD). All six sites have substantial NIDA experience in conducting PC-RCT with cocaine pharmacotherapies. The primary objective of this study is to evaluate the efficacy of two different doses of TA-CD (100 or 400 ug) versus placebo to increase the number of cocaine-free days across treatment groups in cocaine-dependent patients. Secondary objectives of this study are: to evaluate safety and tolerability of five injections of TA-CD, to evaluate immunogenicity of TA-CD, to investigate any correlation between change in levels of cocaine use, craving, or subjective effects of cocaine and antibody levels, and finally, to examine predictors of treatment response. Previous work with the TA-CD vaccine has shown both doses (100 and 400 ug) and a regimen of 5 injections over 12 weeks are clinically safe and produce substantial levels of anti-cocaine antibody. During a previous PC-RCT, cocaine abusers with these anti-cocaine antibodies (AB) substantially reduced their smoked cocaine and had a significant reduction in overall cocaine use. That study also showed an expected variation in AB levels was a determinant of therapeutic response (e.g. higher AB levels were associated with a greater reduction in cocaine use). That previous PC-RCT provided effect size data for calculating the sample size of 300 with a potential dropout of up to 30%. In order to enhance retention in this 16-week study, we will use contingency management (CM), which in a pilot study provided outstanding retention of over 80% for a 16 week study. To complete this study within a 3 year period and have reasonable accrual and retention of this difficult population requires participation of six sites. These six extremely well-qualified research groups have comparable and complementary skills that can examine innovative ways to deliver a medical therapy through vaccination. The six sites are: Baylor College of Medicine (BCM), (lead); University of Cincinnati; Johns Hopkins University; University of Pennsylvania; New York University; and, Columbia University. All of these collaborators are working with the pharmaceutical manufacturer--Celtic, and NIDA to help with data management and laboratory-processing for quantitative urine toxicology. PUBLIC HEALTH RELEVANCE: New approaches are needed to help treat those addicted to cocaine to successfully keep from relapsing to drug abuse after withdrawal. Vaccines that stimulate strong antibody responses against cocaine will help such individuals by blocking the drug craving that occurs after re-exposure to cocaine in someone who has been abstinent. This research will define ways to make and effectively use such vaccines to stimulate high antibody levels that will have the best chance of success.
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Human methamphetamine vaccine: Translational Avante Garde Award
  • 批准号:
    8289239
  • 项目类别:
  • 资助金额:
    $78.25万
  • 财政年份:
    2011
  • 负责人:
    THOMAS Richard KOSTEN
  • 依托单位:
Human methamphetamine vaccine: Translational Avante Garde Award
  • 批准号:
    9137114
  • 项目类别:
  • 资助金额:
    $6.4万
  • 财政年份:
    2011
  • 负责人:
    THOMAS Richard KOSTEN
  • 依托单位:
Human methamphetamine vaccine: Translational Avante Garde Award
  • 批准号:
    8724467
  • 项目类别:
  • 资助金额:
    $78.25万
  • 财政年份:
    2011
  • 负责人:
    THOMAS Richard KOSTEN
  • 依托单位:
Human methamphetamine vaccine: Translational Avante Garde Award
  • 批准号:
    8540992
  • 项目类别:
  • 资助金额:
    $75.12万
  • 财政年份:
    2011
  • 负责人:
    THOMAS Richard KOSTEN
  • 依托单位:
海外基金