PAS Research | Tampa, FL
Status and phase
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About
The purpose of VAN00010 study is to assess the safety and immunogenicity of the investigational pentavalent meningococcal ABCYW vaccine in adults and adolescents.
The study duration will be up to 12 months for all participants.
Full description
The study duration will be approximately 12 months for all participants
Enrollment
Sex
Ages
Volunteers
Inclusion and exclusion criteria
Inclusion Criteria: - Aged 18 to 25 years or 10 to 17 years on the day of inclusion
Primary purpose
Allocation
Interventional model
Masking
1,220 participants in 7 patient groups
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Central trial contact
Trial Transparency email recommended (Toll free for US & Canada)
Data sourced from clinicaltrials.gov
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