Almirall R&D Centre, Department of Integrative Pharmacology, Barcelona, Spain.
Expert Opin Ther Pat. 2013 Aug;23(8):997-1016. doi: 10.1517/13543776.2013.794789. Epub 2013 May 4.
At last, after many years of research, roflumilast has become the first oral phosphodiesterase-4 inhibitor to be approved by the medical agencies as an add-on therapy for chronic obstructive pulmonary disease. A second compound, apremilast is targeted for submission of new drug application for the treatment of psoriasis in the second half of 2013. These compounds represent a breakthrough and a reward in the field after the many failures to date in clinical development.
This review summarizes the clinical development of PDE4 inhibitors from 2010 - 2012 and the associated patent literature with a focus on strategies to overcome the common pitfalls of oral PDE4 inhibitors.
In the last few years, influenced by the body of published clinical data, many companies have lost interest in PDE4 as a target. Many of those that have persevered have opted to realign their research programs either toward compounds specifically designed for inhaled delivery or in search of an increase in clinical efficacy by combining two mechanisms in a single compound. This change is reflected by the continued disclosure of novel and chemically diverse molecules, indicating for some in the pharmaceutical industry that all is not yet lost.
经过多年的研究,罗氟司特终于成为第一个被医药机构批准的口服磷酸二酯酶-4 抑制剂,作为慢性阻塞性肺疾病的附加疗法。第二种化合物阿普司特的新药申请目标是在 2013 年下半年治疗银屑病。这些化合物是该领域在迄今为止的临床开发中多次失败后的一个突破和回报。
本综述总结了 2010 年至 2012 年 PDE4 抑制剂的临床开发情况及相关专利文献,重点介绍了克服口服 PDE4 抑制剂常见问题的策略。
在过去的几年中,受已发表的临床数据的影响,许多公司对 PDE4 作为靶点失去了兴趣。许多坚持下来的公司选择调整他们的研究计划,要么针对专门用于吸入给药的化合物,要么通过将两种机制结合在单个化合物中以提高临床疗效。这种变化反映在继续披露新的、化学多样性的分子上,这表明对于一些制药行业来说,一切尚未失去。