Spellberg B, Miller L G, Kuo M N, Bradley J, Scheld W M, Edwards J E
Division of Infectious Diseases, Harbor-University of California, Los Angeles Medical Center, and the Los Angeles Biomedical Research Institute, 1124 W. Carson St., Torrance, CA 90502, USA.
Infection. 2007 Jun;35(3):167-74. doi: 10.1007/s15010-007-6269-7.
Over the last two decades, an alarming rise in infections caused by antibiotic-resistant microbes has been paralleled by an equally alarming decline in the development of new antibiotics to deal with the threat. In response to this brewing "perfect storm" of infectious diseases, the Infectious Diseases Society of America (IDSA) has released a white paper that proposes incentives to stimulate critically needed antibiotic development by pharmaceutical companies. A cornerstone of the recommendations is establishment of a "wild-card patent extension" program. This program would allow a company receiving United States (US) Food and Drug Administration (FDA) approval for a new anti-infective agent targeting a drug-resistant pathogen to extend the patent on a drug within their active portfolio. However, wild-card patent extension legislation is highly controversial due to concerns regarding its societal cost.
We performed a systematic literature review to estimate the societal cost of wild-card patent extension compared to the savings resulting from the availability of one new antibiotic to treat multi-drug-resistant Pseudomonas aeruginosa.
We conservatively estimate that wild-card patent extension applied to one new antibiotic would cost $7.7 billion over the first 2 years, and $3.9 billion over the next 18 years. Thus, even if the new antibiotic abrogated only 50% of the annual societal cost of multidrug-resistant P. aeruginosa (estimated $2.7 billion), wild-card patent extension would be cost neutral by 10 years after approval of the new antibiotic, and would save society approximately $4.6 billion by 20 years after approval.
Wild-card patent extension appears to be a cost-effective strategy to spur anti-infective development. Although our analysis is limited by the precision of published data, our model employed conservative assumptions.
在过去二十年中,抗生素耐药微生物引起的感染惊人地增加,与此同时,应对这一威胁的新抗生素研发也出现了同样惊人的下降。为应对这场日益逼近的传染病“完美风暴”,美国传染病学会(IDSA)发布了一份白皮书,提议采取激励措施,以刺激制药公司开展急需的抗生素研发。这些建议的一个基石是建立一个“通配符专利延期”计划。该计划将允许一家因针对耐药病原体的新型抗感染药物获得美国食品药品监督管理局(FDA)批准的公司,延长其现有产品线中一种药物的专利。然而,由于担心其社会成本,通配符专利延期立法极具争议性。
我们进行了一项系统的文献综述,以估计通配符专利延期的社会成本,并与一种用于治疗多重耐药铜绿假单胞菌的新抗生素所带来的节省进行比较。
我们保守估计,应用于一种新抗生素的通配符专利延期在头两年将花费77亿美元,在接下来的18年将花费39亿美元。因此,即使这种新抗生素仅消除了多重耐药铜绿假单胞菌每年社会成本的50%(估计为27亿美元),通配符专利延期在新抗生素获批后10年将实现成本平衡,在获批后20年将为社会节省约46亿美元。
通配符专利延期似乎是促进抗感染药物研发的一种具有成本效益的策略。尽管我们的分析受到已发表数据精度的限制,但我们的模型采用了保守假设。