作者: Tal Zaks
DOI: 10.1007/978-1-60327-088-5_18
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摘要: The elucidation of the human genome sequence and advent genomic technologies have potential to facilitate drug discovery development as well define individual risks benefits associated with specific therapeutic interventions. This chapter focuses on application this knowledge within pharmaceutical industry, by providing current examples relevance both germline somatic genotypic variations adverse event efficacy profiles recently developed anti-cancer drugs. These examples, discussed scientific, regulatory, economic frameworks that shape highlight emerging challenges post-genomic science “real-life” development.