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临床试验/NCT02411942
NCT02411942已完成1 期

A Multi-Center, Double-Blind, Randomized, Placebo Controlled, Parallel-Group Study Comparing Adapalene Gel 0.3% to Differin® (Adapalene Gel 0.3%) and Both Active Treatments to a Placebo Control in the Treatment of Acne Vulgaris

Taro Pharmaceuticals USA0 个研究点目标入组 753 人开始时间: 2014年8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
753
主要终点
Change in inflammatory lesion counts

研究概览

简要总结

The objectives of this study are to evaluate the therapeutic equivalence and safety of Adapalene Gel 0.3% and Differin® (adapalene gel 0.3%).

详细描述

The objectives of this study are to evaluate the therapeutic equivalence and safety of Adapalene Gel 0.3% and Differin® (adapalene gel 0.3%) in the treatment of acne vulgaris and to demonstrate the superiority of the efficacy of the test and reference products over the placebo.

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
Double (Participant, Investigator)

入排标准

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

入选标准

  • Healthy male or non-pregnant female aged ≥ 12 and ≤ 40 years with a clinical diagnosis of acne vulgaris.
  • Subjects aged 18 years and older must have provided written consent. Subjects aged 12 to 17 years must have provided written assent accompanied by written consent from their legally acceptable representative. All subjects or their legally acceptable representatives must sign Health Insurance Portability and Accountability Act authorization.
  • Must have a minimum of ≥ 25 non-inflammatory lesions and ≥ 20 inflammatory lesions and ≤ 2 nodulocystic lesions at baseline on the face.
  • Must have a definite clinical diagnosis of acne vulgaris severity grade 2, 3, or 4 as per the Investigator's Global Assessment.

排除标准

  • Female subjects who are pregnant, nursing or planning to become pregnant during study participation.
  • Have a history of hypersensitivity or allergy to adapalene, retinoids and/or any of the study medication ingredients.
  • Presence of any skin condition that would interfere with the diagnosis or assessment of acne vulgaris.

研究组 & 干预措施

Adapalene Gel 0.3%

Experimental

Adapalene Gel 0.3% (Taro Pharmaceuticals Inc.)

干预措施: Adapalene Gel 0.3% (Drug)

Differin®

Active Comparator

Differin® (adapalene gel 0.3%) (Galderma Laboratories, LP, US)

干预措施: Differin® (Drug)

Placebo

Placebo Comparator

Placebo (vehicle of the test product) (Taro Pharmaceuticals Inc.)

干预措施: Placebo (Drug)

结局指标

主要结局

Change in inflammatory lesion counts

时间窗: Week 12

Percent change from baseline to week 12 in the inflammatory (papules and pustules) lesion counts

Change in non-inflammatory lesion counts

时间窗: Week 12

Percent change from baseline to week 12 in the non-inflammatory (open and closed comedones) lesion counts

次要结局

  • Clinical response of success(Week 12)

研究者

申办方类型
Industry
责任方
Sponsor

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