Advanced Development of the rF1V and rBV A/B Vaccines: Progress and Challenges
Author(s) -
Mary Kate Hart,
George A. Saviolakis,
Susan L. Welkos,
Robert V. House
Publication year - 2011
Publication title -
advances in preventive medicine
Language(s) - English
Resource type - Journals
eISSN - 2090-3499
pISSN - 2090-3480
DOI - 10.1155/2012/731604
Subject(s) - biodefense , medicine , biological warfare , licensure , yersinia pestis , drug approval , virology , biology , pharmacology , toxicology , drug , pathology , biochemistry , nursing , virulence , gene
The development of vaccines for microorganisms and bacterial toxins with the potential to be used as biowarfare and bioterrorism agents is an important component of the US biodefense program. DVC is developing two vaccines, one against inhalational exposure to botulinum neurotoxins A1 and B1 and a second for Yersinia pestis , with the ultimate goal of licensure by the FDA under the Animal Rule. Progress has been made in all technical areas, including manufacturing, nonclinical, and clinical development and testing of the vaccines, and in assay development. The current status of development of these vaccines, and remaining challenges are described in this chapter.
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