drugset / Trial / NCT00057525

A New Anthrax Vaccine Administered by the Intramuscular (IM) Route in Healthy Adults

NCT00057525 ↗

Phase 1 Completed 70 enrolled DynPort Vaccine Company LLC, A GDIT Company
RandomizedSingle-groupDouble-blindPrevention

Summary

This study will provide preliminary safety and comparative immunogenicity data for the E.coli derived rPA vaccine administered by intramuscular (IM) injection at Day 0 and Month 1.Doses will range from 5 μg to 100 μg rPA, and at each dose-level, rPA will either be combined with phosphate-buffered saline (PBS) or adsorbed to Alhydrogel.

Timeline

Start
2003-04
Primary completion
2004-04
Completion
2004-08

Drugs

EvaluationDrugModalityDoseRoute
Subject E. Coli-Derived Recombinant Protective Antigen Unknown 5 ug Intramuscular
Subject E. Coli-Derived Recombinant Protective Antigen Unknown 25 ug Intramuscular
Subject E. Coli-Derived Recombinant Protective Antigen Unknown 50 ug Intramuscular
Subject E. Coli-Derived Recombinant Protective Antigen Unknown 100 ug Intramuscular

Indications