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临床试验/EUCTR2017-003897-15-DE
EUCTR2017-003897-15-DE进行中(未招募)1 期

A Phase 2, randomised, single-masked, active-controlled, multicentre study to evaluate the efficacy and safety of intravitreal THR-317 administered in combination with ranibizumab, for the treatment of diabetic macular oedema (DME)

Oxurion NV0 个研究点目标入组 72 人开始时间: 2018年1月25日最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
Oxurion NV
入组人数
72

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

入选标准

  • - Male or female aged 18 years or older
  • - Type 1 or type 2 diabetes
  • - CI-DME with central subfield thickness of = 320µm on Spectralis® SDOCT
  • or = 305µm on non-Spectralis SD-OCT, in the study eye
  • - Anti-VEGF treatment naïve study eye, or poor or no response to prior
  • treatment with ranibizumab in the study eye
  • - Reduced vision primarily due to DME, with BCVA = 72 and = 23 ETDRS
  • letter score (= 20/40 and = 20/320 Snellen equivalent) in the study eye
  • - Non-proliferative diabetic retinopathy (NPDR) of any stage in the study
  • - Written informed consent obtained from the subject prior to screening
  • 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 36
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 36

排除标准

  • - Macular oedema due to causes other than DME
  • - Concurrent disease in the study eye, other than CI-DME, that could
  • compromise BCVA, require medical or surgical intervention during the study period or could confound interpretation of the results
  • - Change of the retinal architecture in the centre of the macula of the
  • study eye that is likely to preclude improvement in BCVA following the
  • resolution of DME
  • - Previous treatments / procedures as listed below, or their planned /
  • expected use during the study period for up to 30 days after the last
  • study treatment:
  • * Ranibizumab treatment in the study eye (any time for anti-VEGF naïve
  • subjects; 1 month for subjects with a poor or no response to
  • ranibizumab treatment)
  • * Bevacizumab treatment in the study eye (any time for anti-VEGF naïve
  • subjects; 3 months for subjects with a poor or no response to
  • ranibizumab treatment)
  • * Aflibercept treatment in the study eye (any time)
  • * Intraocular surgery in the study eye (3 months)
  • * Focal / grid laser photocoagulation in the study eye (3 months)
  • * Panretinal laser photocoagulation in the study eye (6 months)
  • * Intraocular or peri-ocular corticosteroids in the study eye (4 months)
  • * Ozurdex® (dexamethasone intravitreal implant) in the study eye (6
  • * Other steroid implant in the study eye (any time)
  • * Systemic anti-VEGF treatment (3 months)
  • * Systemic corticosteroids (3 months)
  • - Aphakic study eye
  • - Uncontrolled glaucoma in the study eye
  • - More than 8D high myopia in the study eye
  • - Any active or suspected periocular / ocular / intraocular infection or
  • inflammation in either eye
  • - Untreated diabetes
  • - Glycated haemoglobin A (HbA1c) > 12%
  • - Uncontrolled hypertension in the opinion of the Investigator
  • - Pregnant or lactating female
  • - Female of child-bearing potential not utilising an adequate form of
  • contraception, or planning to become pregnant or to discontinue
  • contraceptive precautions at any time during the entire study period
  • - Male of reproductive potential not utilising contraception

研究者

发起方
Oxurion NV

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