Rostami-Hodjegan Amin, Tucker Geoff
Simcyp Limited, UK.
Simcyp Limited, UK.
Drug Discov Today Technol. 2004 Dec;1(4):441-8. doi: 10.1016/j.ddtec.2004.10.002.
Recently, metabolic drug-drug interactions (M-DDI) have raised some high-profile problems in drug development resulting in restricted use, withdrawal or non-approval by regulatory agencies. The use of in vitro technologies to evaluate the potential for M-DDI has become routine in the drug development process. Nevertheless, in the absence of an integrated approach, their interpretation and value remains the subject of debate, and the vital distinction between a useful "simulation" and a precise "prediction" is not often appreciated. Various in silico softwares are now available for the simulation of M-DDI. However, a concerted effort by the industry is necessary to evaluate their use. The FDA has recently emphasised the importance of such collaboration to improve the crucial path to development of new drugs. In silico simulation of M-DDI has the potential to add significant value to this process.:
最近,代谢性药物相互作用(M-DDI)在药物研发中引发了一些备受瞩目的问题,导致药物使用受限、撤市或未获监管机构批准。在药物研发过程中,使用体外技术评估M-DDI的可能性已成为常规操作。然而,在缺乏综合方法的情况下,对这些技术的解读及其价值仍存在争议,而且人们常常没有认识到有用的“模拟”与精确的“预测”之间的关键区别。现在有各种计算机软件可用于模拟M-DDI。然而,行业需要共同努力来评估它们的用途。美国食品药品监督管理局(FDA)最近强调了这种合作对于改进新药研发关键路径的重要性。M-DDI的计算机模拟有可能为这一过程增添重大价值。