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临床试验/NCT00667173
NCT00667173已完成2 期

A Phase 2, Multi-Center, Evaluator-Blind, Randomized, Vehicle-Controlled Clinical Study to Assess the Safety and Efficacy of IDP-115 in the Treatment of Rosacea

Dow Pharmaceutical Sciences10 个研究点 分布在 1 个国家目标入组 140 人开始时间: 2007年11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
已完成
发起方
入组人数
140
试验地点
10
主要终点
Change from baseline in the number of inflammatory lesions

研究概览

简要总结

The purpose of this study is to assess the safety and effectiveness of IDP-115 in treating patients with rosacea.

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
Single (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

  • Presence of facial rosacea
  • Presence of inflammatory lesions

排除标准

  • Dermatological conditions of the face that could interfere with clinical evaluations
  • Known history of photosensitivity disorders (such as lupus erythematosus or polymorphous light eruption)
  • Female subjects who are pregnant, nursing, planning a pregnancy, or become pregnant during the study

研究组 & 干预措施

1

Experimental

干预措施: IDP-115 (Drug)

2

Placebo Comparator

干预措施: Vehicle (Drug)

3

Placebo Comparator

干预措施: Vehicle (Drug)

结局指标

主要结局

Change from baseline in the number of inflammatory lesions

时间窗: 12 weeks

Improvement from baseline in global severity

时间窗: 12 weeks

次要结局

  • Change from baseline in erythema(12 weeks)

研究者

发起方
Dow Pharmaceutical Sciences
申办方类型
Industry
责任方
Sponsor

研究点 (10)

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