CompletedPhase 1NCT03416036
Evaluation of the Efficacy of the Live Attenuated Tetravalent Dengue Vaccine Against DENV-2 and DENV-3 Challenge
Studying Dengue fever
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- National Institute of Allergy and Infectious Diseases (NIAID)
- Principal Investigator
- Anna Durbin, MD, MDJohns Hopkins Bloomberg School of Public Health
- Intervention
- TetraVax-DV-TV003 (TV003)(biological)
- Enrollment
- 64 enrolled
- Eligibility
- 18-50 years · All sexes
- Timeline
- 2017 – 2019
Study locations (2)
- Center for Immunization Research, Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland, United States
- Vaccine Testing Center, University of Vermont, Burlington, Vermont, United States
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
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