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临床试验/EUCTR2010-022211-19-HU
EUCTR2010-022211-19-HU进行中(未招募)不适用

PILOT STUDY TO EXPLORE EFFICACY AND SAFETY OF DIFFERENT DOSE REGIMENS OF CD5789 IN SUBJECTS WITH ACNE VULGARIS

GALDERMA R&D0 个研究点目标入组 120 人开始时间: 2010年12月6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
GALDERMA R&D
入组人数
120

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
  • •* The Subject has a severity grade of 3 or 4 on the Investigator’s Global Assessment (IGA) scale on either side of the face
  • •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 more than 2 acne nodules/cysts on the face
  • •* The subject has severe forms of acne (acne conglobata, acne fulminans) or secondary acne form (chloracne, drug-induced acne, etc.)
  • •* The number of inflammatory or non inflammatory lesions on half-face is greater than twice the number on the other half-face

研究者

发起方
GALDERMA R&D

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