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按治疗类别划分的新药研发成本。对美国制药行业的一项研究。

Research and development costs for new drugs by therapeutic category. A study of the US pharmaceutical industry.

作者信息

DiMasi J A, Hansen R W, Grabowski H G, Lasagna L

机构信息

Tufts Center for the Study of Drug Development, Tufts University, Boston, Massachusetts, USA.

出版信息

Pharmacoeconomics. 1995 Feb;7(2):152-69. doi: 10.2165/00019053-199507020-00007.

Abstract

The clinical period (i.e. clinical trial and long term animal testing) development costs of a random sample of new chemical entities (NCEs) were examined for differences in average cost. All of the NCEs studied were first tested in humans between 1970 and 1982, and were classified for the purposes of the study by therapeutic class. The costs of unsuccessful projects were included with those of projects that resulted in US marketing approval. Including income forgone from expending funds before returns are earned ('time costs'), the capitalised (i.e. out-of-pocket plus time) clinical period costs per approved NCE were $US70, $US98, $US103 and $US163 million (1993 dollars) for anti-infective, cardiovascular, neuropharmacological and nonsteroidal anti-inflammatory drugs, respectively. Combining the data for all therapeutic categories, the mean clinical period cost per approved NCE was $US93 million. Omitting costs associated with unsuccessful projects, the mean capitalised clinical period costs for approved NCEs ranged from $US7.1 million (for topical steroids) to $US66.7 million (for cardiovascular agents) [1993 dollars]. The estimates of total clinical period costs per approved NCE depend on average out-of-pocket clinical phase costs, attrition rates across phases (i.e. the rates at which compounds drop out of active testing), the probability of marketing approval, and development and regulatory review times. Phase attrition and approval rates are the most important sources of variability in total clinical period costs between therapeutic categories. Development cost estimates by therapeutic category did not correlate strongly with US sales in the fifth year of marketing. Cardiovascular NCEs had much higher than average sales revenues, but clinical development costs for these drugs were only slightly above average. Conversely, nonsteroidal anti-inflammatory drugs attained average sales revenues, but had much higher than average development costs.

摘要

对一组新化学实体(NCEs)随机样本的临床阶段(即临床试验和长期动物试验)开发成本进行了平均成本差异研究。所有研究的NCEs于1970年至1982年间首次在人体进行试验,并根据治疗类别进行分类以便研究。未成功项目的成本与获得美国市场批准的项目成本一同计算。包括在获得回报之前投入资金所放弃的收入(“时间成本”),每种获批NCE的资本化(即自付费用加时间)临床阶段成本,抗感染药物、心血管药物、神经药理学药物和非甾体抗炎药分别为7000万美元、9800万美元、1.03亿美元和1.63亿美元(1993年美元)。综合所有治疗类别的数据,每种获批NCE的平均临床阶段成本为9300万美元。剔除与未成功项目相关的成本后,获批NCE的平均资本化临床阶段成本从710万美元(局部用类固醇)到6670万美元(心血管药物)不等[1993年美元]。每种获批NCE的总临床阶段成本估计取决于平均自付临床阶段成本、各阶段的损耗率(即化合物退出活性测试的速率)、市场批准的概率以及开发和监管审查时间。阶段损耗率和批准率是不同治疗类别之间总临床阶段成本变化的最重要来源。按治疗类别划分的开发成本估计与上市后第五年的美国销售额相关性不强。心血管NCEs的销售收入远高于平均水平,但其临床开发成本仅略高于平均水平。相反,非甾体抗炎药的销售收入处于平均水平,但其开发成本远高于平均水平。

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