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Tuber Lung Dis. 1999;79(3):145-51.

Propelling novel vaccines directed against tuberculosis through the regulatory process.

Author information

1
Laboratory of Mycobacteria, Center for Biologics Evaluation and Research, Food and Drug Administration, Rockville, MD 20852-1448, USA. Brennan@cber.fda.gov

Abstract

The development of novel vaccines for use in the prevention and immunotherapy of tuberculosis is an area of intense interest for scientific researchers, public health agencies and pharmaceutical manufacturers. Development of effective anti-tuberculosis vaccines for use in specific target populations will require close cooperation among several different international organizations including agencies responsible for evaluating the safety and effectiveness of new biologics for human use. In this review, the major issues that are addressed by regulatory agencies to ensure that vaccines are pure, potent, safe, and effective are discussed. It is hoped that the comments provided here will help accelerate the development of new effective vaccines for the prevention and treatment of tuberculosis.

PMID:
10656113
DOI:
10.1054/tuld.1998.0199
[Indexed for MEDLINE]

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