跳至主要内容
临床试验/NCT01048593
NCT01048593终止2 期

A Multicenter, Randomized, Double-masked, Dose-ranging, Phase 2 Study to Evaluate the Efficacy and Safety of IBI-10090 in Cataract Surgery Patients

ICON Bioscience Inc1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2010年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
2 期
状态
终止
入组人数
6
试验地点
1
主要终点
Clearance of Anterior Chamber Cells

研究概览

简要总结

This study will test the efficacy and safety of IBI-10090 for the reduction of ocular inflammation after cataract surgery.

详细描述

All patients received active treatment in this study. Dose group 1 received 114ug of dexamethasone, Dose group 2 received 513ug and Dose group 3 received 684ug.

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
Triple (Participant, Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • Male or female patients 40 years of age scheduled for unilateral cataract surgery (phacoemulsification or extracapsular extraction) with posterior chamber intraocular lens implantation.

排除标准

  • Patients who have used any ocular, topical or oral corticosteroids within 7 days prior to Day
  • Patients who have used topical ocular NSAIDs in the study eye within 15 days prior to screening.
  • Patients with any signs of intraocular inflammation in either eye at screening.
  • Patients who have received any prior intravitreal injections in the study eye.

研究组 & 干预措施

Dose 1

Experimental

114ug

干预措施: IBI-10090 (Drug)

Dose 2

Experimental

513ug

干预措施: IBI-10090 (Drug)

Dose 3

Experimental

684ug

干预措施: IBI-10090 (Drug)

结局指标

主要结局

Clearance of Anterior Chamber Cells

时间窗: Day 8 post treatment

Efficacy was assessed by slit lamp biomicroscopy to evaluate the anterior chamber cells (ACC) graded on a scale of 0 to 4. The primary efficacy endpoint was complete clearing of ACC, where grade 0 = 0 cells in the anterior chamber on POD 8.

次要结局

  • Anterior Chamber Flare (ACF) Grade(Day 90 post-treatment)
  • Anterior Chamber Cell Grade(Day 90 post-treatment)
  • Conjunctival Erythema Grade(Day 90 post-treatment)
  • Corneal Edema Grade(Day 90 post-treatment)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

Loading locations...

相似试验