CompletedPhase 1NCT02684383
Evaluation of the Safety and Immunogenicity of rDEN3Δ30, a Live Attenuated Monovalent Dengue Virus Vaccine
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
- Kristen Pierce, MD, MDUniversity of Vermont
- Intervention
- rDEN3∆30(biological)
- Enrollment
- 14 enrolled
- Eligibility
- 18-50 years · All sexes
- Timeline
- 2016
Study locations (2)
- Center for Immunization Research (CIR), Johns Hopkins School of Public Health, Baltimore, Maryland, United States
- University of Vermont Medical Center, 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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