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临床试验/EUCTR2016-002100-25-CZ
EUCTR2016-002100-25-CZ进行中(未招募)1 期

A Phase 2, single-masked, multicentre study to evaluate the safety and efficacy of 2 dose levels of THR-317 for the treatment of diabetic macular oedema (DME)

ThromboGenics NV0 个研究点目标入组 50 人开始时间: 2016年9月8日最近更新:

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
50

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • Male or female aged 18 years or older
  • Type 1 or type 2 diabetes
  • Centre-involved DME with CST = 340µm on Spectralis spectral domain optical coherence tomography (SD-OCT) or = 320µm on non-Spectralis SD-OCT, in the study eye
  • Reduced vision primarily due to DME, with BCVA between 72 and 23 ETDRS letters read (20/40 and 20/320 Snellen equivalent) in the study eye
  • Anti-VEGF treatment naïve study eye or poor response to prior anti-VEGF treatment in the study eye
  • Non-proliferative diabetic retinopathy (NPDR) or stable proliferative diabetic retinopathy (PDR) without neovacularisation at the disc (NVD)
  • Written informed consent obtained from the subject prior to screening procedures
  • Are the trial subjects under 18? no
  • Number of subjects for this age range:
  • F.1.2 Adults (18-64 years) yes
  • F.1.2.1 Number of subjects for this age range 25
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 25

排除标准

  • Concurrent disease in the study eye, other than DME, that could compromise BCVA, require medical or surgical intervention during the study period or could confound interpretation of the results
  • Previous treatments / procedures as listed below or their planned use during the THR-317 treatment period for up to 30 days after the last injection
  • Treatment / Procedure in Excluded Period prior to
  • the Study Eye Visit 2 (Day 0)
  • Panretinal or focal / grid laser 3 months
  • photocoagulation
  • Anti-VEGF treatment Any time for anti-VEGF naïve
  • subjects; 4 weeks for subjects
  • with a poor response to anti-VEGF
  • Intra-ocular or peri-ocular 4 months
  • corticosteroids
  • Steroid implant Any time
  • Intra-ocular surgery 3 months
  • Vitrectomy Any time
  • Any active ocular / intra-ocular infection or inflammation in either eye
  • Aphakic study eye
  • Untreated diabetes
  • Glycated haemoglobin A (HbA1c) > 12%
  • Uncontrolled hypertension in the opinion of the Investigator
  • Pregnant or lactating female or female of child-bearing potential not utilising an adequate form of contraception or male of reproductive potential not utilising contraception

研究者

发起方
ThromboGenics NV

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