Heinemann Lutz, Hompesch Marcus
Science & Co, Düsseldorf, Germany
Profil Institute for Clinical Research, San Diego, CA, USA.
J Diabetes Sci Technol. 2014 Jan;8(1):6-13. doi: 10.1177/1932296813516958. Epub 2014 Jan 1.
Until now most of the insulin used in developed countries has been manufactured and distributed by a small number of multinational companies. Beyond the established insulin manufacturers, a number of new players have developed insulin manufacturing capacities based on modern biotechnological methods. Because the patents for many of the approved insulin formulations have expired or are going to expire soon, these not yet established companies are increasingly interested in seeking market approval for their insulin products as biosimilar insulins (BI) in highly regulated markets like the EU and the United States. Differences in the manufacturing process (none of the insulin manufacturing procedures are 100% identical) can lead to insulins that to some extent may differ from the originator insulin. The key questions are if subtle differences in the structure of the insulins, purity, and so on are clinically relevant and may result in different biological effects. The aim of this article is to introduce and discuss basic aspects that may be of relevance with regard to BI.
到目前为止,发达国家使用的大多数胰岛素都是由少数跨国公司生产和分销的。除了老牌胰岛素制造商之外,一些新企业已基于现代生物技术方法发展出了胰岛素生产能力。由于许多已获批胰岛素制剂的专利已经过期或即将到期,这些尚未站稳脚跟的公司越来越有兴趣在欧盟和美国等监管严格的市场寻求将其胰岛素产品作为生物类似物胰岛素(BI)的市场批准。生产工艺的差异(没有一种胰岛素生产程序是100%相同的)可能导致胰岛素在某种程度上与原创胰岛素有所不同。关键问题在于胰岛素结构、纯度等方面的细微差异是否具有临床相关性,以及是否可能导致不同的生物学效应。本文的目的是介绍和讨论与生物类似物胰岛素相关的基本方面。