European union regulatory developments for new vaccine adjuvants and delivery systems

Author:

Sesardic Dorothea,Dobbelaer Roland

Publisher

Elsevier BV

Subject

Infectious Diseases,Public Health, Environmental and Occupational Health,General Veterinary,General Immunology and Microbiology,Molecular Medicine

Reference12 articles.

1. Sesardic D, Corbel MJ. Pre-clinical evaluation and quality control aspects of microparticulate antigen delivery systems. In: Gander B, Merkle HP, Corradin H, editors. Antigen delivery systems: immunological and technical issues. Harwood Academic Press; 1997. p. 227–50.

2. Immunological concepts of vaccine adjuvant activity;Schijns;Curr. Opin. Immunol.,2000

3. In IL-4 defficient mice, alum not only generates T-helper-1 responses equivalent to Freund’s complete adjuvant, but continues to induce T helper-2 cytokine production;Brewer;Eur. J. Immunol.,1996

4. The European Pharmacopoeia Commission 2002. English fourth ed. General Monograph: Vaccines for Human Use; 2002: 153.

5. Committee for Proprietary Medicinal Products (CPMP) 1998. Note for Guidance on Pharmaceutical and Biological Aspects of Combined Vaccines (CPMP/BWP/447/97). http://www.emea.eu.int.

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