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Phase I Clinical Trial of SYL040012 a Small Interfering RNA Targeting β-Adrenergic Receptor 2 for Lowering Intraocular Pressure

机译:靶向β-肾上腺素能受体2的小干扰RNA SYL040012降低眼压的I期临床试验

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摘要

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.
机译:这项研究的目的是评估局部耐受的小干扰RNA的眼耐受性,安全性以及对眼内压(IOP)的影响。 SYL040012,关于健康的志愿者。该研究是一项开放性,对照,单中心研究,包括两个区间,分别纳入30名IOP低于21 mmHg的健康受试者。在间隔1期间,将SYL040012以单剂的形式向六只受试者给药。在间隔2中,每天将两只不同剂量的SYL040012分别以7天的时间分别给药于两只眼睛,分别分给12名受试者的两组。对侧眼进行评估,但不进行管理,并作为耐受性研究的对照。 SYL040012在当地耐受良好。在任何研究剂量下均无与产品相关的局部或全身性不良事件。在任何时间点血浆中均未检测到SYL040012。在7天的时间内服用SYL040012可以降低24名健康受试者中15名的IOP值,无论使用何种剂量。响应于所测试的一种剂量,IOP降低在统计学上是显着的,并且基线IOP较高的个体对SYL040012的响应性似乎更大。

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