CompletedPhase 1NCT00097396
Safety, Tolerability & Immunogenicity of the Recombinant Plague Vaccine rF1V
Studying Plague
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
- DynPort Vaccine Company LLC, A GDIT Company
- Principal Investigator
- Richard N Greenberg, MDUniversity of Kentucky
- Intervention
- rF1V vaccine(biological)
- Enrollment
- 40 target
- Eligibility
- 18-40 years · All sexes
- Timeline
- 2004 – 2006
Study locations (1)
- University of Kentucky, Lexington, Kentucky, 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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