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Toxicity studies tissue cross-reactivity testing

Tissue Cross-Reactivity Studies for Monoclonal Antibodies Predictive Value and Use for Selection of Relevant Animal Species for Toxicity Testing... [Pg.207]

Tissue cross-reactivity studies are required by FDA for monoclonal antibody products to determine if the product binds to target and/or nontarget tissues. They are also performed for nonmonoclonal biopharmaceuticals if warranted. For example, ARANESP was tested in a human tissue panel ex vivo to determine if it bound to nontarget tissues or cross-reacted with related cytokine receptors. These studies are also used to explore known or potential clinical adverse safety events (i.e., mechanism of toxicity). For example, one patient in a Raptiva study developed unilateral hearing loss. This finding was further evaluated by cross-reactivity studies with human optic chiasm, acoustic nerve, and inner ear tissues. [Pg.963]


See other pages where Toxicity studies tissue cross-reactivity testing is mentioned: [Pg.214]    [Pg.263]    [Pg.363]    [Pg.56]    [Pg.191]    [Pg.231]    [Pg.232]    [Pg.315]    [Pg.594]    [Pg.964]    [Pg.286]    [Pg.24]    [Pg.182]    [Pg.198]   
See also in sourсe #XX -- [ Pg.963 ]




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