NL-OMON35596已完成2 期
A phase 2, multi-national, multi-centre, double masked, randomised, placebo controlled, parallel-group study to investigate the safety, tolerability, pharmacokinetics, pharmacodynamics and efficacy of darapladib administered for 3 months to adult subjects with diabetic macular edema with centre involvement (DM2115403) - DM2115403
适应症
试验速览
- 阶段
- 2 期
- 状态
- 已完成
- 入组人数
- 10
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional
入排标准
- 年龄范围
- 18 至 99(—)
入选标准
- •* Male and female patients 18 years or above with diabetic macular edema and central involvement.
- •* Confirmation of diagnosis in the study eye by fluorescein angiography.
- •* Retinal thickening > 330 microns for Heidelberg Spectralis and >310 for Zeiss Cirrus.
- •* Best corrected visual acuity score of 78-24 letters (Snellen equivalent ~20/32 to 20/320).
- •* Diabetes mellitus type 1 or 2.
- •* Safe contraception for women of childbearing potential.
排除标准
- •* Additional eye disease in the study eye that could compromise assessments.
- •* Active proliferative diabetic retinopathy in the study eye.
- •* Ischemic maculopathy (see protocol for details).
- •* History of choroidal neovascularization in the study eye, or current choroidal neovascularization in the fellow eye requiring treatment.
- •* Intraocular surgery or laser photocoagulation in the study eye within 3 months of dosing.
- •* Study eye: intravitreal ranibizumab within 90 days or or intraocular steroids within 180 days of dosing.
- •* Fellow eye: (expected need for) intravitreal bevacizumab during the study.
- •* Best-corrected visual acuity score by electronic ETDRS < 56 letters in the fellow eye at screening.
- •* Use of any systemically administered anti-angiogenic agent within 6 months of dosing.
- •* Uncontrolled intraocular pressure >22 mmHg in the study eye despite treatment.
- •* Within 6 months prior to the Screening Visit, use of medications known to be toxic to the retina.
- •* HbA1c >10% at screening.
- •* Severe asthma that is poorly controlled.
- •* Chronic administration of strong CYP3A4 inhibitors.
- •* History of or current chronic use of systemic steroids 30 days or less prior to screening.
- •* Breastfeeding, pregnancy.
研究者
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