Jiam Nicole T, Rauch Steven D
Department of Otolaryngology - Head and Neck Surgery, Harvard Medical School, Massachusetts Eye and Ear, Boston, MA, United States.
Front Neurosci. 2023 Jun 22;17:1169122. doi: 10.3389/fnins.2023.1169122. eCollection 2023.
Despite over 20 years of effort in academic research centers, start-up companies, and established pharmaceutical companies, there are no FDA-approved inner ear therapeutics for treatment of sensorineural hearing loss. There are a number of systemic barriers to creation of this new field of inner ear therapeutics. These include insufficient understanding of the particularity of different causes of hearing loss at the cellular and molecular level, lack of diagnostics of adequate sensitivity and specificity to discern these differences , a tendency for start-up biotech/pharma companies to prioritize competition over collaboration, and a drug development ecosystem that is really in the "pre-competitive" phase and a lack of infrastructure to develop, validate, gain regulatory approval, and successfully market an inner ear therapeutic. These issues will be discussed in this perspective article and a proposed remedy in the form of an inner ear therapeutics "moon shot" will be offered.
尽管学术研究中心、初创公司和老牌制药公司已经付出了20多年的努力,但目前尚无美国食品药品监督管理局(FDA)批准的用于治疗感音神经性听力损失的内耳疗法。创建这个内耳治疗新领域存在许多系统性障碍。这些障碍包括在细胞和分子水平上对不同听力损失原因的特殊性认识不足,缺乏具有足够灵敏度和特异性以辨别这些差异的诊断方法,初创生物科技/制药公司倾向于将竞争置于合作之上,以及药物开发生态系统实际上仍处于“竞争前”阶段,且缺乏开发、验证、获得监管批准并成功销售内耳疗法的基础设施。本文将对这些问题进行讨论,并提出以内耳疗法“登月计划”形式的补救措施。