Pharmacovigilance and Risk Management Sector, European Medicines Agency, London, UK.
Clin Pharmacol Ther. 2012 Apr;91(4):747-50. doi: 10.1038/clpt.2012.4. Epub 2012 Feb 29.
The occurrence of severe adverse events such as progressive multifocal leukoencephalopathy (PML) has the potential to limit the benefits of highly efficacious medicines being developed to fulfill unmet clinical needs across therapeutic areas. Following an Expert meeting in London in July 2011 (http://www.ema.europa.eu/docs/en_GB/document_library/Report/2011/09/WC500111562.pdf), a research agenda, highlighting methodological, clinical, and communication elements, to mitigate the risk and improve the management of drug-induced PML has been agreed upon.
严重不良事件(如进行性多灶性白质脑病,PML)的发生有可能限制正在开发的高效药物的效益,而这些药物是为了满足治疗领域的未满足的临床需求。继 2011 年 7 月在伦敦举行的一次专家会议(http://www.ema.europa.eu/docs/en_GB/document_library/Report/2011/09/WC500111562.pdf)之后,已经达成了一项研究议程,重点强调了减轻药物引起的 PML 的风险和改善其管理所需的方法学、临床和沟通要素。