Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 10:10 PM
Ignite Modification Date:
2025-12-24 @ 10:10 PM
NCT ID:
NCT01502735
Eligibility Criteria:
Inclusion Criteria:
* Males and females 18 years of age or the legal age of consent (whichever is greater) to 50 (inclusive) years of age
* Negative screening laboratory test against dengue, Japanese Encephalitis, West Nile, and Yellow Fever viruses
* Healthy
* All subjects must agree to use contraception or to abstain from sex from enrollment through trial completion
* Able to provide informed consent and able to be followed throughout the trial period
Exclusion Criteria:
* History of Flavivirus infection or history of Flavivirus vaccine (experimental or licensed product) including Japanese encephalitis, West Nile virus, Yellow fever, and dengue
* Have a known or suspected hypersensitivity or adverse reaction to vaccines
* Have received a live-attenuated vaccine within 42 days prior to the initial injection on Day 0 or a subunit or killed vaccine within 30 days of the initial injection on Day 0
* Are pregnant or breastfeeding
* Known HIV, Hepatitis B and/or Hepatitis C infection
* Have any acute illness, including an oral body temperature greater than 100.4°F at the day of vaccination
* Have any occupational, social, or medical concerns that would impact subject safety, interfere with protocol adherence, or affect a subject's ability to give informed consent
* Have been using immunomodulatory therapy (use of systemic corticosteroids or chemotherapeutics that may influence antibody development) within the past 6 months; medications or nutritional supplements known to or which potentially could affect organ function within 30 days prior to the initial injection
* Have received an investigational drug or vaccine or participated in a drug product or vaccine study within a period of 30 days prior to Day 0
* Have received or donated blood or plasma within 90 days of Day 0 (or plan on receiving or donating blood or plasma during the study)
Healthy Volunteers:
True
Sex:
ALL
Minimum Age:
18 Years
Maximum Age:
50 Years
Study:
NCT01502735
Study Brief:
Protocol Section:
NCT01502735