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Mol Ther. 2013 May;21(5):973-85. doi: 10.1038/mt.2013.31. Epub 2013 Feb 26.
2
Pharmacological management of ocular hypertension: current approaches and future prospective.眼高压的药物治疗管理:当前方法与未来展望。
Curr Opin Pharmacol. 2013 Feb;13(1):50-5. doi: 10.1016/j.coph.2012.09.012. Epub 2012 Oct 12.
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Phase 1 dose-escalation study of a siRNA targeting the RTP801 gene in age-related macular degeneration patients.一项针对与年龄相关的黄斑变性患者的 RTP801 基因的 siRNA 靶向药物的 1 期剂量递增研究。
Eye (Lond). 2012 Aug;26(8):1099-105. doi: 10.1038/eye.2012.106. Epub 2012 May 25.
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Epidemiology of major eye diseases leading to blindness in Europe: a literature review.欧洲致盲性主要眼病的流行病学:文献回顾。
Ophthalmic Res. 2012;47(4):171-88. doi: 10.1159/000329603. Epub 2011 Nov 26.
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High-dose siRNAs upregulate mouse Eri-1 at both transcription and posttranscription levels.高剂量的 siRNAs 在转录和转录后水平上调小鼠 Eri-1 的表达。
PLoS One. 2011;6(10):e26466. doi: 10.1371/journal.pone.0026466. Epub 2011 Oct 19.
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Efficiency of glaucoma drug regulation in 5 European countries: a 1995-2006 longitudinal prescription analysis.5 个欧洲国家的青光眼药物监管效率:1995-2006 年的纵向处方分析。
J Glaucoma. 2011 Apr-May;20(4):234-9. doi: 10.1097/ijg.0b013e3181e0791c.
7
Ocular neuroprotection by siRNA targeting caspase-2.靶向半胱氨酸天冬氨酸蛋白酶-2 的 siRNA 对眼部的神经保护作用。
Cell Death Dis. 2011 Jun 16;2(6):e173. doi: 10.1038/cddis.2011.54.
8
Effects of common topical antiglaucoma medications on the ocular surface, eyelids and periorbital tissue.常见局部抗青光眼药物对眼表面、眼睑和眼眶组织的影响。
Drugs Aging. 2011 Apr 1;28(4):267-82. doi: 10.2165/11588830-000000000-00000.
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Medical management of glaucoma: principles and practice.青光眼的医学管理:原则与实践。
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10
A randomized, double-blind, placebo-controlled study of an RNAi-based therapy directed against respiratory syncytial virus.一项针对呼吸道合胞病毒的基于 RNAi 的治疗的随机、双盲、安慰剂对照研究。
Proc Natl Acad Sci U S A. 2010 May 11;107(19):8800-5. doi: 10.1073/pnas.0912186107. Epub 2010 Apr 26.

SYL040012 是一种针对β-肾上腺素能受体 2 的小干扰 RNA 的 I 期临床试验,用于降低眼内压。

Phase I clinical trial of SYL040012, a small interfering RNA targeting β-adrenergic receptor 2, for lowering intraocular pressure.

机构信息

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.

出版信息

Mol Ther. 2014 Jan;22(1):226-32. doi: 10.1038/mt.2013.217. Epub 2013 Sep 12.

DOI:10.1038/mt.2013.217
PMID:24025752
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3978811/
Abstract

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.

摘要

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。