drugset / Trial / NCT05065983

A Study to Assess the Safety and Immunogenicity of PXVX0317 Chikungunya Virus Virus-Like Particle Vaccine

NCT05065983 ↗

Phase 2 Completed 25 enrolled Bavarian Nordic Emergent BioSolutions · collab
NaSingle-groupOpen-labelPrevention

Summary

The objective of this study is to assess the safety and immunogenicity of PXVX0317 (Chikungunya Virus Virus-Like Particle Vaccine \[CHIKV VLP\], aluminum hydroxide adjuvanted).

Timeline

Start
2021-10-11
Primary completion
2022-05-05
Completion
2022-05-05

Drugs

EvaluationDrugModalityDoseRoute
Subject PXVX0317 Vaccine 40 ug —

Indications