Reichert Janice M
Tufts Center for the Study of Drug Development, Boston, MA 02111, USA.
Trends Biotechnol. 2006 Jul;24(7):293-8. doi: 10.1016/j.tibtech.2006.05.003. Epub 2006 Jun 6.
The efficient development and approval of new therapeutics and vaccines is vital to the health and welfare of patients. Tufts Center for the Study of Drug Development has collected and analyzed data for new protein therapeutics and vaccines approved in the USA during the past decade. Our results suggest trends toward longer clinical and approval phases for the therapeutics, particularly for oncology products. In this Opinion article, we discuss various legislative acts and FDA initiatives that might improve the efficiency of drug development and approval. Furthermore, few new vaccines have been approved in the past 10 years owing, at least in part, to the lack of incentives for the development of the products. We predict that this might change in the future as government and industry respond to the twin threats of the global spread of infectious diseases and potential bioterrorism.
新疗法和疫苗的高效研发与获批对患者的健康和福祉至关重要。塔夫茨药物研发研究中心收集并分析了过去十年间在美国获批的新型蛋白质疗法和疫苗的数据。我们的结果显示,这些疗法,尤其是肿瘤学产品,呈现出临床和获批阶段延长的趋势。在这篇观点文章中,我们讨论了各种可能提高药物研发和获批效率的立法法案及美国食品药品监督管理局的举措。此外,过去十年间获批的新疫苗很少,这至少部分归因于产品研发缺乏激励措施。我们预测,随着政府和行业应对传染病全球传播和潜在生物恐怖主义这两大威胁,这种情况未来可能会改变。