Phase 3 Trial Evaluates Safety and Immunogenicity of CHIKV VLP Vaccine in Children
Summary
A Phase 3 trial is assessing the safety and immunogenicity of the CHIKV VLP vaccine in children aged 1 to <12 years. Primary endpoints include the incidence of AESI, MAAEs, and SAEs, and the seroresponse rate on Day 22 in seronegative children.
Researchers are studying a new vaccine for chikungunya virus in children. They want to see if it is safe and helps the body build protection against the virus.
Monitor for updates on CHIKV VLP vaccine's safety and immunogenicity in children.
CT.gov
Drug Pipeline
Phase3
n=720
Mar 2026
Phase3
n=720
Mar 2026