CompletedPhase 2NCT00350337

Safety and Immunogenicity of Various Formulations of Live Attenuated Tetravalent Dengue Vaccine in Healthy US Adults

Studying Dengue fever

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
U.S. Army Medical Research and Development Command
Principal Investigator
Stephen J Thomas, MD, FACP
Walter Reed Army Institute of Research (WRAIR)
Intervention
Pre-transfection F17(biological)
Enrollment
86 enrolled
Eligibility
18-45 years · All sexes
Timeline
20062008

Study locations (1)

Collaborators

GlaxoSmithKline · Walter Reed Army Institute of Research (WRAIR)

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.

Open NCT00350337 on ClinicalTrials.gov

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