Reichert Janice M
Senior Research Fellow, Tufts University, Tufts Center for the Study of Drug Development, 75 Kneeland Street, Suite 1100, Boston, MA 02111, USA.
Curr Pharm Biotechnol. 2008 Dec;9(6):423-30. doi: 10.2174/138920108786786358.
Monoclonal antibodies (mAbs) comprise the majority of protein candidates currently in clinical development because of their versatility as therapeutic agents. While traditionally associated with the biotechnology industry, mAb therapeutics are now being developed and marketed by most major pharmaceutical firms. A total of 21 products are approved in the US, with additional products marketed outside the US, and over 200 mAb candidates are currently undergoing clinical study. Benchmark data for mAb therapeutics, such as clinical development and US Food and Drug Administration approval times, approval success rates, and clinical phase transition probabilities, are critical for strategic planning purposes. Trends in these benchmarks for various types of mAbs, with an emphasis on those studied as anticancer and immunological therapeutics, are discussed.
单克隆抗体(mAb)由于其作为治疗药物的多功能性,构成了目前处于临床开发阶段的大多数蛋白质候选药物。虽然传统上与生物技术行业相关,但单克隆抗体疗法现在正由大多数大型制药公司进行开发和销售。在美国共有21种产品获批,在美国以外地区也有其他产品上市,目前有200多种单克隆抗体候选药物正在进行临床研究。单克隆抗体疗法的基准数据,如临床开发和美国食品药品监督管理局(FDA)的批准时间、批准成功率以及临床阶段转换概率,对于战略规划目的至关重要。本文讨论了各类单克隆抗体在这些基准方面的趋势,重点是作为抗癌和免疫治疗药物进行研究的单克隆抗体。