跳至主要内容
临床试验/NCT07592585
NCT07592585招募中3 期

Phase III Clinical Study to Evaluate the Efficacy and Safety of VC005 in Adult and Adolescents With Mild to Moderate Atopic Dermatitis

Jiangsu vcare pharmaceutical technology co., LTD1 个研究点 分布在 1 个国家目标入组 360 人开始时间: 2026年5月12日最近更新:
适应症
干预措施

试验速览

阶段
3 期
状态
招募中
入组人数
360
试验地点
1

研究概览

简要总结

A multicenter, randomized, double-blind, vehicle controlled phase III clinical study to evaluate the efficacy and safety of VC005 in adults and adolescents with mild to moderate atopic dermatitis

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 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Subjects fully understand this study, are able to follow the relevant procedures of the trial, voluntarily participate in the clinical trial, and sign the informed consent form (ICF);
  • The age requirement for signing the ICF is 12 years old or above, with no gender restrictions;
  • During screening, the diagnosis of atopic dermatitis should be met according to the Hanifin-Rajka criteria.

排除标准

  • Patients whose AD course is judged by the investigator as unstable(spontaneous improvement or rapid worsening) within 2 weeks prior to baseline;
  • At screening and baseline, lesions are localized only to the hands or feet, with no prior history of involvement of other typical areas (such as the face or flexural areas);
  • Skin damage or abnormalities that may affect the evaluation of the investigational drug administration site (e.g., pigmentation, extensive scarring, tattoos, etc., at the affected area);
  • At screening and baseline, presence of skin diseases that may affect the evaluation of the administration site, including but not limited to: psoriasis, acne, skin cancer, generalized erythroderma, Netherton syndrome, etc.

研究组 & 干预措施

VC005 Placebo group

Placebo Comparator

干预措施: VC005 Placebo (Drug)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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