CompletedPhase 1NCT01666652

A Two-dose Primary Vaccination Study of a Tetravalent Dengue Virus Purified Inactivated Vaccine vs. Placebo in Healthy 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
Leyi Lin, MD
Walter Reed Army Institute of Research (WRAIR)
Intervention
4 µg TDENV-PIV with Alum adjuvant(biological)
Enrollment
100 enrolled
Eligibility
18-39 years · All sexes
Timeline
2012 – 2017

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 NCT01666652 on ClinicalTrials.gov

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