Active, not recruitingPhase 3NCT04838444
Antibody Persistence And Long Term Safety Of A Chikungunya Virus Vaccine (VLA1553)
Studying Chikungunya
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Valneva Austria GmbH
- Principal Investigator
- Valneva Clinical DevelopmentValneva Austria GmbH
- Intervention
- VLA1553(biological)
- Enrollment
- 363 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2021 – 2031
Study locations (10)
- Accelerated Enrollment Solutions (AES), Phoenix, Arizona, United States
- Velocity Clinical Research, Hallandale, Florida, United States
- Accelerated Enrollment Solutions (AES), Chicago, Illinois, United States
- Alliance for Multispecialty Research (AMR), Lexington, Kentucky, United States
- Velocity Clinical Research, Grand Island, Nebraska, United States
- Velocity Clinical Research, Omaha, Nebraska, United States
- Alliance for Multispecialty Research (AMR), Knoxville, Tennessee, United States
- Velocity Clinical Research, Austin, Texas, United States
- Velocity Clinical Research, West Jordan, Utah, United States
- Allliance for Multispecialty Research (AMR), Norfolk, Virginia, United States
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.
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