Bryant Laura M, Christopher Devin M, Giles April R, Hinderer Christian, Rodriguez Jesse L, Smith Jenessa B, Traxler Elizabeth A, Tycko Josh, Wojno Adam P, Wilson James M
Neuroscience Graduate Group, University of Pennsylvania, Philadelphia, PA 19104, USA.
Hum Gene Ther Clin Dev. 2013 Jun;24(2):55-64. doi: 10.1089/humc.2013.087. Epub 2013 Jun 29.
Bryant and colleagues follow the development of Glybera (alipogene tiparvovec), the first gene therapy product approved in the European Union, from early preclinical studies through the approval process. They review key data from human and animal studies with an emphasis on issues that will be critical to other gene therapy products. The article concludes with an analysis of the complex review process that eventually led to Glybera's approval.
布莱恩特及其同事追踪了欧洲首个获批的基因治疗产品Glybera(alipogene tiparvovec)从早期临床前研究到获批过程的发展历程。他们回顾了来自人体和动物研究的关键数据,重点关注对其他基因治疗产品至关重要的问题。文章最后分析了最终促成Glybera获批的复杂审评过程。