跳至主要内容
临床试验/NCT03452527
NCT03452527终止2 期

A Phase 2 Randomized, Open-Label, Multicenter Study Evaluating Administration of Repeated Intravitreal Doses of ICON-1 in Patients With Choroidal Neovascularization Secondary to Age-related Macular Degeneration

Iconic Therapeutics, Inc.16 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2018年3月26日最近更新:
适应症

试验速览

阶段
2 期
状态
终止
入组人数
15
试验地点
16
主要终点
Change in Choroidal Neovascularization (CNV) Over Time

研究概览

简要总结

The purpose of this study is to evaluate the safety and effects of repeated intravitreal injections of ICON-1 0.6 mg administered as maintenance therapy or in combination with aflibercept in patients with wet macular degeneration.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
None

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Males or females of any race, ≥50 years of age
  • Active primary CNV secondary to AMD in the study eye

排除标准

  • Any prior treatment of CNV or advanced AMD in the study eye, except for dietary supplements or vitamins
  • Any intraocular or ocular surface surgery (including cataract surgery and laser procedures) in the study eye within 3 months
  • Vitrectomy in the study eye

结局指标

主要结局

Change in Choroidal Neovascularization (CNV) Over Time

时间窗: Month 9

Mean change from baseline in CNV area in the study eye

次要结局

  • Change in Best Corrected Visual Acuity (BCVA) Over Time(Month 9)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (16)

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