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Application of drug metabolism and pharmacokinetics for new drug development

机译:药物代谢和药代动力学在新药开发中的应用

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Preclinical drug discovery is a time- and labor-consuming work and unfortunately very small number of compounds can be applicable to patients. Moreover, though the cost of new drug development has been increasing for the past many years, the number of approved new drug is relatively fixed (Kola and Landis, 2004). Theoretically it is not possible to develop new drug with complete safety and high efficacy, so the pharmaceutical companies always try to pre-screen potential toxicity of drug candidates. Approximately 50% of lead compounds failed because of insufficient efficacy and 40% attrition of lead compounds is due to safety issues (DiMasi, 1995).
机译:临床前药物发现是一项费时费力的工作,不幸的是,非常少量的化合物可用于患者。此外,尽管在过去的几年中开发新药的成本一直在增加,但批准的新药的数量却相对固定(Kola and Landis,2004)。从理论上讲,不可能开发出具有完全安全性和高功效的新药,因此制药公司总是试图预先筛选候选药物的潜在毒性。约有50%的铅化合物由于功效不足而失败,而40%的铅化合物损耗是由于安全问题(DiMasi,1995)。

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