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Clinical Trial Summary

The trial investigates Px563L and RPA563, two formulations of a novel anthrax vaccine.


Clinical Trial Description

This is a Phase 1, double-blind, randomized, placebo-controlled study to evaluate the safety, tolerability, and immunogenicity of Px563L or RPA563 administered intramuscularly. All subjects will be followed for safety and tolerability for 393 days after the initial vaccination. Immunogenicity analyses will be performed for up to 182 days, including an interim analysis based on Day 70 results, after the initial vaccination. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02655549
Study type Interventional
Source Pfenex, Inc
Contact
Status Completed
Phase Phase 1
Start date December 2015
Completion date June 2017

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