Study in Healthy Volunteers Evaluating Safety and Pharmacokinetics of Zika Virus Immune Globulin (ZIKV-IG)
NCT03624946
Arbovirus Infections, Flaviviridae Infections
Toronto, Ontario, Canada
View Trial DetailsNCT Number: NCT03158233
This prospective, surveillance study will assess the operational Zika virus definition for use in future Zika purified inactivated virus (ZIKV) vaccine efficacy trials in order to identify Zika virus disease (ZVD) cases among the study cohort.
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Notify Me15 year–40 year
All sexes
Observational
Investigational Site, Floridablanca, Santander Department, Colombia
This prospective, multicenter, cohort study will conduct active and passive surveillance for ZVD and determine its prevalence and seroconversion incidence in areas of Latin America experiencing Zika epidemic activity. A description of the occurrence of dengue virus and chikungunya virus infections in the cohort may also be provided as differential diagnosis of ZVD.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
For subjects at or over the age of majority on the day of inclusion: the informed consent form has been signed and dated.
Time frame: Day 0 to Day 365
Number of suspected ZVD and VCZ infections
Time frame: Day 0 to Day 365
Occurrence, intensity, and duration of signs and symptoms of ZVD and VCZ cases
Sanofi Pasteur, a Sanofi Company
Industry
Prospective Surveillance and Case Definition Study of Zika Virus Disease and Infection in Adolescents and Adults in Latin America in Preparation for an Efficacy Trial of a Zika Virus Whole Virion, Purified Inactivated Vaccine
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