drugset / Trial / NCT06973772

Trial to Evaluate the Immunogenicity and Safety of the Co-administration of Live Attenuated Dengue and Chikungunya Vaccines Compared to Separate Administration in Adults Aged 18 to 59 Years.

NCT06973772 ↗

Phase 3 Not yet recruiting 900 enrolled Butantan Institute
RandomizedParallel-groupTriple-blindPrevention

Summary

This randomized, controlled, double blind trial aims at assessing the safety and immunogenicity profiles of the co-administered Live Attenuated Dengue and Chikungunya vaccines comparatively to the isolated administration, in the adult population aged 18 to 59 years without prior exposure to either arbovirus.

Timeline

Start
2027-03-31
Primary completion
2027-07
Completion
2027-10

Publications

Drugs

EvaluationDrugModalityDoseRoute
Subject Butantan-DV Vaccine — Subcutaneous
Subject VLA1555 Vaccine 3 unknown Intramuscular