CompletedPhase 1NCT03922061
Evaluation of Safety, Reactogenicity and Immunogenicity of Fractional-dose Inactivated Polio Vaccine (fIPV) Given Intradermally With Double Mutant Enterotoxigenic Escherichia Coli Heat Labile Toxin (dmLT) Adjuvant
Studying Poliomyelitis
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
- University of Vermont
- Principal Investigator
- Kelly Cowan, M.D.University of Vermont
- Intervention
- dmLT(biological)
- Enrollment
- 29 target
- Eligibility
- 18-45 years · All sexes
- Timeline
- 2019 – 2020
Study locations (1)
- University of Vermont, Burlington, Vermont, 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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