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临床试验/NCT01987323
NCT01987323已完成1 期

Safety and Efficacy of Liposomal Latanoprost in Ocular Hypertensive Patients

Singapore Eye Research Institute0 个研究点目标入组 6 人开始时间: 2013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
已完成
入组人数
6
主要终点
Number of participants with serious adverse events

研究概览

简要总结

Aim: Evaluation of a single subconjunctival injection of liposomal EggPC formulation of latanoprost in treating glaucoma.

Hypothesis: The investigators have already evaluated carrier stability, drug partitioning, in vitro drug release, tolerance, and efficacy of latanoprost-incorporated EggPC liposomes upon subconjunctival administration in both rabbit and monkey eyes. Therefore, the investigators hypothesize that this would be safe and efficacious in humans as well.

Methodology: A pilot study to assess a liposome formulation containing latanoprost. The investigators will recruit 6 study subjects with eyes that have raised IOP, for subconjunctival injection of this liposome formulation. The recruited eye will be injected and monitored for inflammation, toxicity and pain as primary end-points. Monitoring of the eye will be for the first 24 hours post-injection, week 2, months 1, 2 and 3 thereafter.

Importance: If proven safe, this method of drug delivery could potentially be used for treatment of raised intraocular pressures in blinding conditions such as glaucoma.

详细描述

The number of recorded adverse events and intolerance to the subconjunctival injection procedure by the participants during the study period was used as a measure of safety.

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
21 Years 至 80 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Glaucoma patients who have eyes with raised IOP (baseline IOP >21 mmHg) due to end-stage glaucoma with a poor visual prognosis.
  • Exclusion criteria:
  • Active or recent eye infection, endophthalmitis
  • Known hypersensitivity to latanoprost
  • Previous glaucoma filtration surgeries or trabeculectomy
  • Intraocular pressure less than 12mmHg.
  • Inability to give informed consent.
  • Inability to safely administer a subconjunctival injection
  • Uncontrolled systemic hypertension, CVA or TIA within the previous month.
  • Pregnancy -

排除标准

  • 未提供

研究组 & 干预措施

Lipolat

Experimental

Subconjunctival injection of Lipolat into the superior bulbar conjunctiva of all enrolled participants

干预措施: Subconjunctival injection of liposomal latanoprost (Drug)

结局指标

主要结局

Number of participants with serious adverse events

时间窗: 3 months

次要结局

  • intraocular pressure(3 months)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

A/Prof Tina Wong

Associate Professor

Singapore Eye Research Institute

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