CompletedPhase 3NCT05349617

Safety and Immunogenicity of CHIKV VLP Vaccine PXVX0317 in Adults ≥65 Years

Studying Chikungunya

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
Bavarian Nordic
Principal Investigator
Patrick Ajiboye, MD
Bavarian Nordic
Intervention
CHIKV VLP/adjuvant(biological)
Enrollment
413 enrolled
Eligibility
65 years · All sexes
Timeline
20222023

Study locations (10)

Collaborators

Emergent BioSolutions

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 NCT05349617 on ClinicalTrials.gov

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