CompletedPhase 1NCT01436422
Evaluating the Safety and Immune Response to Two Admixtures of a Tetravalent 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
- Anna Durbin, MD, MDCenter for Immunization Research (CIR), Johns Hopkins School of Public Health
- Intervention
- TetraVax-DV Vaccine - Admixture TV003(biological)
- Enrollment
- 112 enrolled
- Eligibility
- 18-50 years · All sexes
- Timeline
- 2011 – 2014
Study locations (3)
- Center for Immunization Research, Johns Hopkins School of Public Health, Baltimore, Maryland, United States
- Fletcher Allen Health Care (FAHC), General Clinical Research Center (GCRC), Burlington, Vermont, United States
- University of Vermont Vaccine Testing 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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