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Study identifier: NCT07467707 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

An Efficacy, Safety, and Immunogenicity Study of CHIKV VLP Vaccine for the Prevention of Chikungunya Disease in Adolescents and Adults

Condition: Chikungunya Virus  ·  Sponsor: Bavarian Nordic

PhasePhase 3
Planned participants6144
Who can joinAll sexes, 12 Years to no upper limit
Healthy volunteersYes

About this study

Study EBSI-CV-317-007 is a field study to evaluate the efficacy, immunogenicity, and safety of CHIKV VLP vaccine. The study was designed using infectious disease models and advanced analytics to guide region and clinical site prioritization, define the timing of study activities, and optimize the study parameters to local epidemiological conditions for CHIKV disease to overcome the challenges of assessing efficacy for CHIKV VLP vaccine.

This description comes directly from the study's public registry record.

Talk to the study team

Anjali Chudasama, MPH M.Sc.  ·  844-422-8274  ·  info@bavarian-nordic.com

Tiffany Brockington  ·  info@bavarian-nordic.com

Always discuss trial participation with your own doctor first.

Locations (3)

WRAIR-AFRIMS Philippines, Cebu (WRAIR-APC)Cebu City, Cebu, PhilippinesRecruiting
Kamphaeng Phet Provincial HospitalKamphaeng Phet, Changwat Kamphaeng Phet, ThailandRecruiting
Songklanagarind hospital, Prince of Songkla University (PSU)Hat Yai, Changwat Songkhla, ThailandNot Yet Recruiting

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Source record: clinicaltrials.gov/study/NCT07467707