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临床试验/EUCTR2015-003991-56-LV
EUCTR2015-003991-56-LV进行中(未招募)1 期

A Phase 2b Randomized, Double-Masked, Controlled Trial to Assess the Safety and Efficacy of Intravitreous Administration of Zimura™ (Anti-C5 Aptamer) in Subjects with Geographic Atrophy Secondary to Dry Age-Related Macular Degeneration

OPHTHOTECH CORPORATIO0 个研究点目标入组 277 人开始时间: 2018年1月3日最近更新:
适应症

试验速览

阶段
1 期
状态
进行中(未招募)
发起方
入组人数
277

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

  • Ophthalmic Inclusion Criteria
  • The following inclusion criteria apply to the SE:
  • - Non-foveal GA secondary to dry AMD.
  • - The atrophic lesion must be able to be photographed in its entirety.
  • - Best corrected visual acuity in the SE between 20/25 – 20/320, inclusive.
  • General Inclusion Criteria
  • - Subjects of either gender aged =50 years.
  • - Women must be using two forms of effective contraception, be post-menopausal for at least 12 months prior to trial entry, or surgically sterile; if of child-bearing potential, a serum pregnancy test must be performed within 14 days prior to the first injection with a negative result. The two forms of effective contraception must be implemented during the trial and for at least 60 days following the last dose of test medication.
  • - Provide written informed consent.
  • - Ability to return for all trial visits.
  • 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 70
  • F.1.3 Elderly (>=65 years) yes
  • F.1.3.1 Number of subjects for this age range 207

排除标准

  • Exclusion Criteria
  • Subjects will not be eligible for the trial if subjects cannot attend all trial required visits, or if any of the following criteria are present systemically or in the SE:
  • Ophthalmic Exclusion Criteria
  • The following exclusion criteria apply to the SE:
  • - Evidence of CNV in either eye.
  • - Any prior treatment for AMD or any prior intravitreal treatment for any indication in either eye, except oral supplements of vitamins and minerals.
  • - Presence of other causes of choroidal neovascularization.
  • - Any intraocular surgery or thermal laser within 3 months of trial entry. Any prior thermal laser in the macular region, regardless of indication.
  • - Any ocular or periocular infection (including blepharitis), or ocular surface inflammation in the past 12 weeks.
  • - Any sign of diabetic retinopathy in either eye.

研究者

发起方
OPHTHOTECH CORPORATIO

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