Ameri Hossein, Kesavamoorthy Niranjana, Bruce Dara N
Department of Ophthalmology, USC Roski Eye Institute, Keck School of Medicine, University of Southern California, Los Angeles, CA 90033, USA.
Biomedicines. 2023 Nov 23;11(12):3124. doi: 10.3390/biomedicines11123124.
The purpose of this study is to describe worldwide gene therapy clinical trials aimed at treating ophthalmic disorders. Information regarding all worldwide clinical trials was collected through 15 different sources, including ClinicalTrials.gov. There were 159 gene therapy clinical trials on ophthalmic diseases up until 2022. Phase 1/2 trials had the highest frequency (50-32%), followed by phase 2 (33-21%); 107 trials (67%) were conducted in a single country, and 50 trials (31%) were multinational. Overall, the USA was the site of 113 (71%) single or multinational trials. Of the trials, 153 (96%) targeted retina and optic nerve disorders, 3 (2%) glaucoma, 2 (1%) uveitis, and 1 (1%) cornea; 104 trials (65%) employed gene augmentation using viral vectors, and the remaining employed other methods such as inhibitory RNA (18-11%) and cell-based gene therapy using encapsulated cell technology (18-11%). For gene augmentation trials, adeno-associated virus was used for transgene delivery in 87% of cases. The most common conditions targeted by gene augmentation included inherited retinal (74%) and age-related macular degeneration (wet, 14%; dry, 7%). Overall, a large number of gene therapy clinical trials have been conducted in the eye, and so far, one has led to regulatory approval.
本研究的目的是描述全球范围内旨在治疗眼科疾病的基因治疗临床试验。通过包括ClinicalTrials.gov在内的15个不同来源收集了有关全球所有临床试验的信息。截至2022年,有159项针对眼科疾病的基因治疗临床试验。1/2期试验的频率最高(50 - 32%),其次是2期试验(33 - 21%);107项试验(67%)在单个国家进行,50项试验(31%)是跨国试验。总体而言,美国是113项(71%)单中心或多中心试验的开展地点。在这些试验中,153项(96%)针对视网膜和视神经疾病,3项(2%)针对青光眼,2项(1%)针对葡萄膜炎,1项(1%)针对角膜;104项试验(65%)使用病毒载体进行基因增强,其余试验采用其他方法,如抑制性RNA(18 - 11%)和使用封装细胞技术的基于细胞的基因治疗(18 - 11%)。对于基因增强试验,87%的病例使用腺相关病毒进行转基因递送。基因增强最常针对的疾病包括遗传性视网膜疾病(74%)和年龄相关性黄斑变性(湿性,14%;干性,7%)。总体而言,已经在眼部进行了大量的基因治疗临床试验,到目前为止,有一项已获得监管批准。