EUCTR2012-003589-42-DE
进行中（未招募）
不适用
Observational (non-interventional), follow-up trial assessing long-term local tolerability and efficacy (recurrence rate) of resiquimod gel in patients treated for actinic keratosis.
概览
- 阶段
- 不适用
- 干预措施
- 未指定
- 疾病 / 适应症
- Actinic Keratosis
- 发起方
- Spirig Pharma AG
- 入组人数
- 80
- 状态
- 进行中（未招募）
- 最后更新
- 11年前
概览
简要总结
暂无简介。
研究者
入排标准
入选标准
- •Signed informed consent.
- •Participation in the previous clinical trial SP848\-AK\-1101\.
- •Patient with complete clinical clearance (i.e. no previously existing AK\-lesion present) at the end of the trial SP848\-AK\-1101 or Non\-Responder who withdrew from the trial prematurely.
- •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 30
- •F.1\.3 Elderly (\>\=65 years) yes
- •F.1\.3\.1 Number of subjects for this age range 50
排除标准
- •Evidence of unstable or uncontrolled clinically significant medical conditions as determined by the investigator (e.g., cardiovascular, immunological, hematologic, hepatic, neurologic, renal, endocrine, collagen\-vascular, infectious, gastrointestinal abnormalities or diseases).
- •Evidence of systemic cancer.
- •Dermatological disease or condition in the former treatment or surrounding area that might
- •impair trial assessments (e.g., rosacea, atopic dermatitis, eczema) as assessed by the investigator.
结局指标
主要结局
未指定
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