Awardee OrganizationUNIV OF NORTH CAROLINA CHAPEL HILL
Description
Abstract Text
Abstract
The University of North Carolina (UNC) Global HIV Prevention and Treatment Clinical Trials Unit
(CTU) has a well-established record of high quality, innovative clinical research, strong network
and scientific leadership. The CTU engages with critically important populations infected with and
at high risk of HIV in southeastern US, southern Africa and southeast Asia. Our CTU is led by
three experienced principal investigators (Joseph Eron MD, Mina Hosseinipour MD and David
Wohl MD) and will support all four NIH Clinical TrialsNetworks (CTN); Adult Therapeutic
Strategies, HIV Prevention, Vaccine Prevention and Pediatric, Adolescent and Maternal
Therapeutic Strategies. Our four experienced Clinical Research Sites (CRS) include Chapel Hill
CRS (Adult Strategies, Prevention and Vaccine CTN) led by Dr. Wohl, Greensboro CRS (Adult
Strategies, Prevention and Vaccine CTN) led by Cornelius Van Dam MD, Malawi CRS (all four
CTN) led by Lameck Chinula MD and Vietnam CRS (Adult Strategies, Prevention and Vaccine
CTN) led by Vivian Go PhD. Participants with HIV include those newly diagnosed (including with
acute infection), PWH stably suppressed on therapy and PWH with adherence challenges to care
or medication and those with drug-resistant HIV. At-risk populations include men who have sex
with men (MSM) including young men of color, transgender women (TGW), people who
inject drugs (PWID) and African adolescent girls and women including those who are pregnant.
We will enroll PWH at risk for comorbidities and PWH or without HIV with co-epidemic pathogens
such as tuberculosis (TB) and Hepatitis B virus (HBV). We have skilled, experienced clinical and
translational investigators working hand-in-hand with junior investigators with diversity of gender
and race, in US and international settings, who will engage and execute the network scientific
agenda. A globally representative set of senior scientists and public health leaders on our
Scientific and Strategic Advisory Group advise the CTU leadership team. The CTU administration
has a highly organized structure that is responsive to our research teams and CRSs. Each CRS
engages the communities representing the affected populations in an interactive, open-minded
way. State-of-art communication and experienced, outstanding and well-organized laboratory,
pharmacy, regulatory, quality and data management support the CTU, CRSs. Using this robust
framework the UNC Global CTU is positioned optimally to continue our scientific, and network
leadership and clinical trials support to the agenda of all four NIH HIV networks.
Public Health Relevance Statement
Project Narrative
The NIH established collaborative HIV/AIDS Clinical TrialsNetworks to advance the science of
HIV prevention and treatment and to contribute to the end of the HIV epidemic. The UNC Global
HIV Treatment and Prevention Clinical Trials Unit will contribute to the work of all four NIH HIV
Clinical TrialsNetworks by enrolling those populations most affected by HIV and by providing
innovate scientific leadership and by contributing to the leadership of the networks.
NIH Spending Category
No NIH Spending Category available.
Project Terms
AIDS preventionAdherenceAdolescentAdultAffectAfricaAfricanAreaCaringCellsChildChildhoodClinicalClinical InvestigatorClinical ResearchClinical TreatmentClinical TrialsClinical TrialsNetworkClinical Trials Support UnitClinical Trials UnitCollaborationsCommunicationCommunitiesComplexDedicationsDevelopmentDisease remissionDoctor of PhilosophyDrug KineticsDrug resistance in tuberculosisEnrollmentEpidemicFemale AdolescentsGoalsHBV cureHIVHIV AntibodiesHIV drug resistanceHIV vaccineHIV/AIDSHIV/HBVHIV/TBHepatitis BHepatitis B VirusIncidenceIndividualInfantInjecting drug userInternationalInterventionInvestigationLaboratoriesLeadLeadershipMalawiMindMother-to-child HIV transmissionNational Institute of Allergy and Infectious DiseaseNewly DiagnosedNorth CarolinaNucleosidesParticipantPatient RecruitmentsPersonsPharmaceutical PreparationsPharmacy facilityPhasePopulationPopulations at RiskPositioning AttributePregnant WomenPreventionPrevention trialPrincipal InvestigatorPublic HealthRaceRecording of previous eventsResearchResearch PersonnelRiskSamplingScienceScientistSenior ScientistSoutheastern AsiaSouthern AfricaTalentsTestingTherapeuticTherapeutic Clinical TrialTuberculosisTuberculosis VaccinesUnited States National Institutes of HealthUniversitiesVaccine Clinical TrialVaccinesVietnamVirusVirus ActivationWorkacute infectionadolescent womanantiretroviral therapyblack womenclinical research siteco-infectioncommunity engagementcomorbiditydata managementearly phase trialexperiencefollow-upgender diversityhigh riskhigh risk populationinnovationmen of colormen who have sex with mennovelorganizational structureparticipant retentionpathogenphase 3 studypre-exposure prophylaxispregnantprevention clinical trialrecruitskillstransgender womentranslational scientisttreatment as preventiontreatment trialvaccine trialviral reboundvirtualvolunteeryoung manyoung men who have sex with menyoung woman
National Institute of Allergy and Infectious Diseases
CFDA Code
855
DUNS Number
608195277
UEI
D3LHU66KBLD5
Project Start Date
01-February-2007
Project End Date
30-November-2027
Budget Start Date
01-December-2024
Budget End Date
30-November-2025
Project Funding Information for 2025
Total Funding
$2,444,748
Direct Costs
$1,229,613
Indirect Costs
$1,215,135
Year
Funding IC
FY Total Cost by IC
2025
National Institute of Allergy and Infectious Diseases
$2,444,748
Year
Funding IC
FY Total Cost by IC
Sub Projects
No Sub Projects information available for 5UM1AI069423-19
Publications
Publications are associated with projects, but cannot be identified with any particular year of the project or fiscal year of funding. This is due to the continuous and cumulative nature of knowledge generation across the life of a project and the sometimes long and variable publishing timeline. Similarly, for multi-component projects, publications are associated with the parent core project and not with individual sub-projects.
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Outcomes
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Clinical Studies
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