At a glance
ClinicalIndex Comparison RecordStandardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Controlled Study of Immunogenicity and Safety of the Investigational vYF Candidate Vaccine in Comparison to YF-VAX in Adults
In Brief
A Phase 2 clinical trial evaluating Yellow fever vaccine (produced on serum-free Vero cells) and Yellow fever vaccine for Yellow Fever and Healthy Volunteers. Active but no longer recruiting, targeting 568 participants across 11 sites.
Detailed Summary
The primary objective of the study is to demonstrate the non-inferiority of the antibody response in terms of seroconversion rate 28 days after vaccine administration of one dose of yellow fever vaccine (vYF) compared to the antibody response after one dose of the YF-VAX control vaccine in yellow fever naïve participants. The secondary objectives of the study are: * To describe the immune response to yellow fever in both vaccine groups before and after vYF or YF-VAX administration. * To describe the safety profile of vYF vaccine in comparison to the safety profile of the control YF-VAX. * To describe the biosafety profile of vYF in comparison to the biosafety profile of the control YF-VAX.
Study Details
Timeline
Interventions
Powder and diluent for suspension for injection Subcutaneous injection
Powder and diluent for suspension for injection Subcutaneous injection