跳至主要内容
临床试验/NCT01177644
NCT01177644撤回1 期

Safety and Preliminary Efficacy Study of PDS-1.0 in Patients With Neovascular AMD

Forsight Vision40 个研究点开始时间: 2011年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
撤回
发起方
主要终点
Change in retinal thickness measured by Optical Coherence Tomography

研究概览

简要总结

This study will evaluate the safety and preliminary effectiveness of PDS 1.0 in patients with neovascular AMD.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Diagnosis of CNV secondary to AMD confirmed by fluorescein angiography, not previously treated
  • Retinal thickness due to edema of at least 300um in the study eye
  • Best corrected visual acuity of 20/80 or worse in the study eye
  • Best corrected visual acuity of 20/40 or better in the fellow eye

排除标准

  • Evidence of scarring CNV (e.g. geographic atrophy) in the study eye
  • Fibrosis >75% of lesion area in the study eye

研究组 & 干预措施

Active

Experimental

干预措施: PDS 1.0 (Drug)

结局指标

主要结局

Change in retinal thickness measured by Optical Coherence Tomography

时间窗: Monthly

次要结局

  • Change in Best Corrected Visual Acuity(Monthly)

研究者

发起方
Forsight Vision4
申办方类型
Industry
责任方
Sponsor

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