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This is a phase 1 trial, consisting of an initial open-label sentinel run-in (n=25) phase and a randomized, double-blind, dose-finding trial (n=125) in flavivirus naΓ―ve adults aged 18 to 49 years. In total Γ’β¬Β¦ In november 2025 positive results of its phase 1 clinical trial investigating the safety and immunogenicity of vla1601 were announced.
Several new strategies are under investigation for vaccines, monoclonal antibodies, and serological tests with improved speciΓ―Β¬Βcity, including multiplex and point-of-care diagnostics.