Schimmer Joshua, Breazzano Steven
Piper Jaffray & Co. , New York, New York.
Hum Gene Ther Clin Dev. 2015 Dec;26(4):208-10. doi: 10.1089/humc.2015.29004.sch.
Spark Therapeutics recently reported positive phase III results for SPK-RPE65 targeting the treatment of visual impairment caused by RPE65 gene mutations (often referred to as Leber congenital amaurosis type 2, or LCA2, but may include other retinal disorders), marking an important inflection point for the field of gene therapy. The results highlight the ability to successfully design and execute a randomized trial of a gene therapy and also reinforce the potentially predictive nature of early preclinical and clinical data. The results are expected to pave the way for the first approved gene therapy product in the United States and should sustain investor interest and confidence in gene therapy for many approaches, including retina targeting and beyond.
Spark Therapeutics公司最近公布了针对由RPE65基因突变导致的视力障碍(通常称为2型莱伯先天性黑蒙,即LCA2,但可能包括其他视网膜疾病)的SPK-RPE65疗法的积极III期试验结果,这标志着基因治疗领域的一个重要转折点。这些结果凸显了成功设计并开展基因治疗随机试验的能力,同时也强化了早期临床前和临床数据的潜在预测性。这些结果有望为美国首个获批的基因治疗产品铺平道路,并应能维持投资者对包括视网膜靶向及其他领域在内的多种基因治疗方法的兴趣和信心。