drugset / Trial / NCT04786444

Study to Demonstrate Consistency of Three Lots of a Live-attenuated Chikungunya Virus Vaccine Candidate in Healthy Adults

NCT04786444

Phase 3 Completed 409 enrolled Valneva Austria GmbH
RandomizedParallel-groupDouble-blindPrevention

Summary

This was a prospective, randomized, double-blinded, multicenter Phase 3 clinical study investigating three Lots of VLA1553 at the final dose. Overall 409 healthy subjects aged 18 to 45 years were randomized into the study.

Timeline

Start
2021-02-22
Primary completion
2021-07-22
Completion
2022-01-26

Drugs

EvaluationDrugModalityDoseRoute
Comparator VLA1553 Vaccine Intramuscular

Indications