Condition: Chickenpox · Sponsor: GlaxoSmithKline
The purpose of this study is to evaluate the immune response and safety of GSKs investigational varicella vaccine (VNS Vaccine) compared to an already approved varicella vaccine, Varivax (VV), when administered as second dose to healthy children. 3 months after first dose at 12 to 15 months. The study will be conducted in children who have not previously contracted varicella or received a varicella vaccination.
This description comes directly from the study's public registry record.
US GSK Clinical Trials Call Center · 877-379-3718 · GSKClinicalSupportHD@gsk.com
EU GSK Clinical Trials Call Center · +44 (0) 20 89904466 · GSKClinicalSupportHD@gsk.com
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| GSK Investigational Site | Salvaleón de Higüey, La Altagracia Province, Dominican Republic | Recruiting |
| GSK Investigational Site | Constanza, Dominican Republic | Recruiting |
| GSK Investigational Site | Santo Domingo Oeste, Dominican Republic | Recruiting |
| GSK Investigational Site | San Pedro Sula, Honduras | Recruiting |
| GSK Investigational Site | Tegucigalpa, Honduras | Recruiting |
| GSK Investigational Site | Tegucigalpa, Honduras | Recruiting |
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Source record: clinicaltrials.gov/study/NCT06806137