grant

The MW Cancer Prevention Clinical Trials Network

Organization UNIVERSITY OF WISCONSIN-MADISONLocation MADISON, UNITED STATESPosted 3 Sept 2020Deadline 31 Jul 2026
NIHUS FederalResearch GrantFY2024AccelerationAdvanced CancerAdvanced Malignant NeoplasmAlaska IndianAlaska NativeAlaskan AmericanAlaskan IndianAlaskan NativeAlaskan Native AmericanAwardBiologicalBiological MarkersBody TissuesCancer BurdenCancer CenterCancer PatientCancer Prevention TrialCancer TreatmentCancersChemopreventionChemopreventiveChemopreventive AgentClinicClinicalClinical ChemopreventionClinical EvaluationClinical TestingClinical TrialsClinical Trials NetworkCollaborationsDevelopmentDivision of Cancer PreventionDoseDysplasiaEpidemiological dataEpidemiology dataFormulationFundingGenetic PredispositionGenetic Predisposition to DiseaseGenetic SusceptibilityGenetic propensityGoalsGroups at riskHistologicHistologicallyHistoryImmunochemical ImmunologicImmunologicImmunologicalImmunologicallyImmunologicsImmunopreventionIndividualIndividuals from minorityIndividuals of minorityInfrastructureInherited PredispositionInherited SusceptibilityInstitutionInterventionIntervention StrategiesInvestigatorsInvestmentsLeadMalignant Neoplasm TherapyMalignant Neoplasm TreatmentMalignant NeoplasmsMalignant TumorMedical centerMinority GroupsMinority PeopleMinority PopulationMinority individualMolecular TargetNCI OrganizationNational Cancer BurdenNational Cancer InstituteNeoplasmsOrganOrganizational AffiliationParticipantPatientsPb elementPeople at riskPerformancePersons at riskPharmacodynamicsPhasePopulationPopulations at RiskPositionPositioning AttributePreventative measurePreventionPrevention programPrevention trialPreventivePreventive measurePrincipal InvestigatorProcessProductivityPuerto RicoRecommendationRecording of previous eventsReproducibilityResearchResearch PersonnelResearchersRiskScienceScreening procedureSiteSpecial PopulationSpecialtyTestingTimeTissuesUnderrepresented Ethnic MinorityUnderrepresented MinorityUniversitiesVaccinesWisconsinanti-cancer therapyanti-carcinogenicanticarcinogenicbio-markersbiologicbiologic markerbiomarkercancer carecancer chemopreventioncancer clinical trialcancer preventioncancer progressioncancer therapycancer-directed therapychemoprevention agentclinical effectclinical relevanceclinical significanceclinical testclinically relevantclinically significantcost effective measuresdesigndesigningdevelopmentaldrug repositioningdrug repurposingdyscrasiaepidemiologic dataexperiencefirst in manfirst-in-humangenetic etiologygenetic mechanism of diseasegenetic vulnerabilitygenetically predisposedhealthy volunteerheavy metal Pbheavy metal leadhigh riskhigh risk grouphigh risk individualhigh risk peoplehigh risk populationhistoriesimprovedinnovateinnovationinnovativeinterventional strategymalignancymedical specialtiesmembermultidisciplinaryneoplasianeoplasm progressionneoplasm/cancerneoplastic growthneoplastic progressionnoveloncology clinical trialphase 1 trialphase I trialpilot trialpreventpreventingprevention clinical trialrepurposing agentrepurposing medicationresearch clinical testingscreening toolstargeted agenttumor progressionunder-representation of minoritiesunder-represented minorityunderrepresentation of minoritiesvaccination studyvaccination trialvaccine studyvaccine trial
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Full Description

ABSTRACT
The need to provide safe and cost-effective measures to prevent Cancer is self-explanatory. The University of

Wisconsin (UWISC) as the Lead Academic Organization (LAO) together with our collaborating institutions

(Affiliated Organizations/AOs) propose to continue performing early phase cancer prevention trials, for the

National Cancer Institute (NCI), Division of Cancer Prevention (DCP), as a Cancer Prevention Clinical Trials

Network (CP-CTNET) site funded as a UG1 Consortium as described in RFA-CA-18-031. Our overarching goal

is to evaluate the effects of novel preventive agents/interventions on pertinent biological endpoints in order to

efficiently determine their appropriateness for further testing and potential viability toward becoming

recommended societal interventions to lessen the burden of cancer. We will pursue this overarching goal via

the following specific aims: (1) Efficiently design, conduct and perform Phase 0, 1, 2 Chemoprevention Clinical

Trials of novel and/or re-purposed immunologic-based or molecular targeted agents, assessing their effects upon

relevant biological (biomarkers/clinical effects) endpoints. (2) Build upon existing consortium infrastructure to

complete Aim 1 via intra- or inter-consortium (CP-CTNET) multi-institutional collaborations in concert with

NCI/DCP contributing three to four new Phase 0, 1 or 2 clinical trials and accrual of ≥ 40-50 subjects per year.

We are well positioned to successfully achieve the above aims due to our combined experience with prevention

agent development (consortium members currently hold >90 DCP sponsored R, U or PREVENT awards) and

our consortium's staffing, organization, and management which results in the timely development, performance

and completion of impactful, multi-institutional early phase cancer prevention trials. Our enhanced consortium

consists of >10 NCI-designated Cancer Centers, institutions providing access to robust numbers of at-risk

patients (e.g. Mayo Clinics, Seattle Cancer Care Alliance) and expanded access to at-risk under-represented

minorities and special populations (e.g. University of Puerto Rico, Alaska Native Medical Center). Supported by

the Carbone Cancer Center, the University of Wisconsin CP-CTNet site is determined to contribute to advancing

the field of Cancer prevention through performance of early phase prevention trials.

Grant Number: 5UG1CA242635-05
NIH Institute/Center: NIH

Principal Investigator: Lisa Barroilhet

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