跳至主要内容
临床试验/NCT07179055
NCT07179055招募中2 期

An Eight-Week, Double-Masked, Randomized, Placebo-Controlled, Phase 2, Evaluation of the Safety and Efficacy of VSJ-110 Ophthalmic Solution in the Treatment of Dry Eye

Vanda Pharmaceuticals1 个研究点 分布在 1 个国家目标入组 160 人开始时间: 2025年10月1日最近更新:
适应症
干预措施

试验速览

阶段
2 期
状态
招募中
入组人数
160
试验地点
1
主要终点
Corneal Staining

研究概览

简要总结

The purpose of this study is to determine the safety and efficacy of VSJ-110 compared to placebo in the treatment of dry eye.

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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Be at least 18 years of age of either gender and any race.
  • Provide written informed consent and sign the HIPAA form.
  • Be willing and able to follow all instructions and attend all study visits.

排除标准

  • Use of any of the disallowed medications during the washout and study period.

研究组 & 干预措施

VSJ-110 Solution

Experimental

干预措施: VSJ-110 (Drug)

Placebo Solution

Placebo Comparator

干预措施: Placebo (Drug)

结局指标

主要结局

Corneal Staining

时间窗: Measured over an 8-week treatment period

Corneal Staining will be assessed by the investigator on a scale of 0-4, with a higher number indicating a higher grade of staining.

次要结局

  • Schirmer's Tear Test(Measured over an 8-week treatment period)
  • Eye Dryness Score (EDS) of the Visual Analogue Scale (VAS)(Measured over an 8-week treatment period)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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