Department of Opthalmology, Facultad de Medicina, Universidad de Navarra, Pamplona, Spain.
Department of Pharmacology and Clinical Investigational Unit, Facultad de Medicina, Universidad de Navarra, Pamplona, Spain.
Mol Ther. 2014 Jan;22(1):226-32. doi: 10.1038/mt.2013.217. Epub 2013 Sep 12.
The objective of this study was to evaluate ocular tolerance, safety, and effect on intraocular pressure (IOP) of a topically administered small interfering RNA; SYL040012, on healthy volunteers. The study was an open-label, controlled, single-center study comprised of two intervals that enrolled 30 healthy subjects having IOP below 21 mmHg. SYL040012 was administered to one eye as a single dose to six subjects during interval 1. During interval 2 two different doses of SYL040012 were administered to one eye on a daily basis to two separate groups of 12 subjects each, over a period of 7 days. The contralateral eye was evaluated but not administered and served as control for the tolerance study. SYL040012 was well tolerated locally. No local or systemic adverse events related to the product developed in response to any of the doses studied. SYL040012 was not detected in plasma at any time point. Administration of SYL040012 over a period of 7 days reduced IOP values in 15 out of 24 healthy subjects regardless of the dose used. IOP decrease was statistically significant in response to one of the doses tested and responsiveness to SYL040012 seemed to be greater in individuals with higher baseline IOP.
本研究旨在评估局部给予小干扰 RNA(SYL040012)对健康志愿者的眼耐受性、安全性和对眼压(IOP)的影响。该研究为一项开放标签、对照、单中心研究,包括两个间隔期,共纳入 30 名 IOP 低于 21mmHg 的健康受试者。在间隔期 1 中,将 SYL040012 单次剂量施用于 6 名受试者的一只眼。在间隔期 2 中,每天将两种不同剂量的 SYL040012 施用于 12 名受试者的一只眼,持续 7 天。对另一眼进行评估但不给予药物,作为耐受性研究的对照。SYL040012 局部耐受性良好。在任何剂量下,均未出现与产品相关的局部或全身不良反应。在任何时间点均未在血浆中检测到 SYL040012。在 7 天的治疗期间,无论使用何种剂量,24 名健康受试者中有 15 名的 IOP 值降低。在一项剂量测试中,IOP 下降具有统计学意义,并且对 SYL040012 的反应似乎在基线 IOP 较高的个体中更大。