EUCTR2010-024214-54-HU进行中(未招募)不适用
Exploratory study to assess facial tolerability after daily application of several concentrations and formulations containing CD5789 in acne subjects
GALDERMA R&D SNC0 个研究点目标入组 60 人开始时间: 2011年5月31日最近更新:
适应症
相关药物
试验速览
- 阶段
- 不适用
- 状态
- 进行中(未招募)
- 发起方
- 入组人数
- 60
研究概览
简要总结
暂无简介。
研究设计
- 研究类型
- Interventional clinical trial of medicinal product
入排标准
- 性别
- All
入选标准
- •Male or female subject aged from 18 to 35 years old
- •The subject has medical diagnosis of moderate to severe acne vulgaris on the face
- •The subject has, on the face, at least 20 inflammatory lesions and 30 non-inflammatory lesions
- •If female of childbearing potential,she agrees to use a highly effective double-barrier contraception method for the duration of the study and one month after the last product application.
- •Are the trial subjects under 18? no
- •Number of subjects for this age range:
- •F.1.2 Adults (18-64 years) yes
- •F.1.2.1 Number of subjects for this age range
- •F.1.3 Elderly (>=65 years) no
- •F.1.3.1 Number of subjects for this age range
排除标准
- •The subject has severe forms of acne requiring systemic treatment (acne conglobata, acne fulminans) or secondary acne form (chloracne, drug-induced acne, etc.)
- •The subject has a known allergy or sensitivity to any of the components of the study products
研究者
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