evidENT, Ear Institute, University College London, Royal National Throat Nose and Ear Hospital.
National Institute of Health Research University College London Hospitals Biomedical Research Centre, London, UK.
Otol Neurotol. 2019 Jun;40(5):559-570. doi: 10.1097/MAO.0000000000002194.
To provide an overview of biotechnology and pharmaceutical companies active in the field of inner ear and central hearing disorders and their therapeutic approaches.
Scientific and grey literature was searched using broad search terms to identify companies and their hearing-related therapeutic approaches. For each approach its lead indication, product, therapeutic modality, target, mechanism of action and current phase of clinical development was collated.
A total of 43 biotechnology and pharmaceutical companies have been identified that are developing therapeutics for inner ear and central hearing disorders. Their therapeutics include drug-, cell- and gene-based approaches to prevent hearing loss or its progression, restore hearing, and regenerate the inner ear. Their therapeutic targets and specific mechanisms of action are wide-ranging, reflecting the complexity of the hearing pathways and the diversity of mechanisms underlying inner ear disorders. While none of the novel products under investigation have yet made it to the clinical market, and a large proportion are still at preclinical phase, many therapeutics have already entered clinical testing with more expected to do so in the next few years.
A wide range of novel therapeutics targeting different hearing, balance and tinnitus pathways, and patient populations are approaching the clinical domain. It is important that clinicians involved in the care of patients with hearing loss prepare for what may become a radically different approach to the management of hearing disorders, and develop a true understanding of the new therapies' mechanisms of action, applications, and indications.
概述在耳内和中枢听力障碍领域活跃的生物技术和制药公司及其治疗方法。
使用广泛的搜索词搜索科学和灰色文献,以确定公司及其与听力相关的治疗方法。对于每种方法,都整理了其主要适应症、产品、治疗方式、靶点、作用机制和当前临床开发阶段。
共确定了 43 家生物技术和制药公司正在开发用于治疗内耳和中枢听力障碍的疗法。他们的疗法包括药物、细胞和基因治疗方法,以预防听力损失或其进展、恢复听力和内耳再生。他们的治疗靶点和具体作用机制多种多样,反映了听力通路的复杂性和内耳疾病的多种潜在机制。虽然没有一种正在研究的新型产品已经进入临床市场,而且很大一部分仍处于临床前阶段,但许多疗法已经进入临床测试,预计未来几年还会有更多的疗法进入临床测试。
针对不同的听力、平衡和耳鸣途径以及患者群体的广泛新型疗法正在进入临床领域。对于涉及听力损失患者护理的临床医生来说,为可能出现的听力障碍管理的全新方法做好准备,并真正了解新疗法的作用机制、应用和适应症非常重要。