Not yet recruitingPhase 3NCT07467707

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

Studying Chikungunya

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Bavarian Nordic
Principal Investigator
Patrick Ajiboye, MD
Bavarian Nordic A/S
Intervention
CHIKV VLP vaccine(biological)
Enrollment
6144 enrolled
Eligibility
12 years · All sexes
Timeline
20262030

Study locations (3)

Collaborators

Walter Reed Army Institute of Research (WRAIR) · Congressionally Directed Medical Research Programs · United States Department of Defense · Pharmaceutical Product Development, (PPD) LLC · Armed Forces Research Institute of Medical Services · Q-square Business Intelligence, Inc.

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT07467707 on ClinicalTrials.gov

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