drugset / Trial / NCT01317667

Safety and Immunogenicity Study of Recombinant Ricin Toxin A-Chain Vaccine (RVEc™)

NCT01317667 ↗

RandomizedParallel-groupOpen-labelOther

Summary

This study is a Phase 1, escalating, multiple-dose, single-center study to evaluate the safety and immunogenicity of the RVEc vaccine. The two principal hypotheses to be tested are: RVEc vaccine will display an acceptable safety profile as determined by adverse event data and RVEc vaccine will elicit ELISA immunoglobulin G (IgG) titers greater than or equal to 1:500 and toxin-neutralizing antibody (TNA) anti-ricin toxin-neutralizing antibody titers greater than or equal to 1:50 in vaccine recipients.

Timeline

Start
2011-03
Primary completion
2012-11
Completion
2014-12

Drugs

EvaluationDrugModalityDoseRoute
Subject RVEc Vaccine 20 ug —
Subject RVEc Vaccine 50 ug —
Subject RVEc Vaccine 100 ug —

Indications