Uslaner Jason M, Herring William J, Coleman Paul J
Discovery Neuroscience, Clinical Neuroscience, and Chemistry, Merck & Co., Inc., Kenilworth, New Jersey 07033, United States.
ACS Pharmacol Transl Sci. 2020 Jan 28;3(1):161-168. doi: 10.1021/acsptsci.9b00110. eCollection 2020 Feb 14.
The development of therapeutics for central nervous system (CNS) disorders has many challenges that result in low probability of success and longer-than-typical development timelines. Suvorexant (Belsomra), the first dual orexin receptor antagonist used for insomnia, was approved by the United States Food and Drug Administration ∼10 years after the initial high-throughput screen was conducted to identify orexin receptor antagonists. What accounted for this success and speed? Here we suggest that this program was unique and set up for success by (1) having a robust and high-throughput pharmacodynamic readout that was translatable across species, including humans, (2) a well-validated target with a defined product profile, resulting in a highly energized team with a can-do attitude, and (3) a highly executable and streamlined clinical strategy. The utility of Belsomra for insomnia, as well as other neurological and psychiatric diseases, continues to be explored, most recently for insomnia associated with Alzheimer's disease.
中枢神经系统(CNS)疾病治疗药物的研发面临诸多挑战,导致成功概率低且研发周期比通常情况更长。苏沃雷生(Belsomra)是首个用于失眠治疗的双重食欲素受体拮抗剂,在最初进行高通量筛选以鉴定食欲素受体拮抗剂约10年后,才获得美国食品药品监督管理局的批准。促成这一成功和速度的因素是什么?在此我们认为,该项目具有独特性且具备成功的条件,原因如下:(1)拥有强大且可跨物种(包括人类)转化的高通量药效学读数;(2)有一个经过充分验证且产品特性明确的靶点,从而打造出一支态度积极、充满活力的团队;(3)拥有高度可执行且精简的临床策略。Belsomra对失眠以及其他神经和精神疾病的效用仍在持续探索中,最近正在研究其对与阿尔茨海默病相关的失眠的疗效。