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临床试验/JPRN-jRCT2080224538
JPRN-jRCT2080224538已完成3 期

Efficacy and safety of LEO 90100 foam in Japanese subjects with psoriasis vulgaris

EO Pharma K.K.0 个研究点目标入组 182 人开始时间: 2019年1月31日最近更新:
适应症

试验速览

阶段
3 期
状态
已完成
发起方
入组人数
182

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional

入排标准

年龄范围
>= 20age old 至 ot applicable(—)
性别
All

入选标准

  • 1.Japanese subjects aged 20 years or more
  • 2.Clinical diagnosis of psoriasis vulgaris of less than or equal to 30% BSA (excluding any psoriasis on the face, skin folds, genitals)
  • 3.A target psoriasis lesion on the body, of a minimum size of 10 cm2 and scoring at least 2 (mild) for each of redness, thickness and scaliness
  • 4.Females of childbearing potential must have a negative result for a urine pregnancy test at Day 1 (Visit 1) and must agree to use an adequate method of birth control

排除标准

  • 1. Use of systemic treatment with an effect on psoriaisis
  • 2. Use of UV therapy on full body or on the target lesion
  • 3. Use of topical treatment on areas to be treated with trial medication
  • 4. Topical treatment on areas other than treated areas with vitamin D
  • analogues, immunosuppressants or strong/very strong corticosteroids
  • 5. Skin diseases besides psoriasis on the areas to be treated with trial medication.
  • 6. Disorders of calcium metabolism, hypercalcaemia, renal insufficiency, hepatic disorders, heart disease.

研究者

发起方
EO Pharma K.K.

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