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Immunogenicity studies preclinical safety evaluation

Immunogenicity is a substantial complication for preclinical safety assessment studies. Antibodies can invalidate the animal model species. Antibody production alone, however, should not necessarily prohibit the conduct of these studies. The effect on pharmacokinetics and pharmcodynamics needs to be measured and evaluated. The potential consequences of the antibodies on endogenous molecules also needs to be evaluated. Secondary effects, such as antibody deposition, should be measured. The lack of ability to predict absolute human immunogenicity does not preclude the use of animals to assess the relative potential for an immune response. [Pg.117]


See other pages where Immunogenicity studies preclinical safety evaluation is mentioned: [Pg.358]    [Pg.491]    [Pg.734]    [Pg.195]    [Pg.220]    [Pg.94]    [Pg.126]    [Pg.150]    [Pg.639]    [Pg.172]    [Pg.697]    [Pg.379]    [Pg.345]    [Pg.381]    [Pg.284]   
See also in sourсe #XX -- [ Pg.60 , Pg.657 ]




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