ISRCTN29254828已完成1 期
A Phase I, randomized, double-blind, placebo-controlled, multiple-dose platform study investigating the immunopharmacology of EDP1815 and EDP2939
Evelo Biosciences0 个研究点目标入组 38 人开始时间: 2022年7月1日最近更新:
适应症
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- 入组人数
- 38
研究概览
简要总结
2024 Results article in https://pubmed.ncbi.nlm.nih.gov/38748319/ (added 24/05/2024)
研究设计
- 研究类型
- Interventional
入排标准
- 性别
- All
入选标准
- •1. Capable of giving signed informed consent, and willing to comply with requirements of the study
- •2. Age 18 years to 45 years, inclusive
- •3. Body mass index of 18 to 35 kg/m2, inclusive
- •4. Caucasian
- •5. Healthy based on medical history, physical examination, blood pressure, ECG and blood and urine laboratory tests
排除标准
- •1. Use of Aldara® (imiquimod cream) within 3 weeks prior to the study
- •2. Has previously received Immucothel® or KLH
- •3. Allergy to Alhydrogel® or Aldara® (imiquimod cream)
- •4. Current or recurrent skin diseases affecting the arms or back, or extensive tattoos in these areas
- •5. Previous diagnosis of psoriasis
- •6. History of pathological scar formation (e.g. keloid scar)
- •7. History of skin cancer (basal cell carcinoma, squamous cell carcinoma, melanoma)
- •8. Significant bowel disease (e.g. inflammatory bowel disease, coeliac disease)
- •9. Currently has an infection or has needed antibiotics within 6 weeks before the study
- •10. Current smoker of more than 5 cigarettes per day
- •11. Tanning due to sunbathing, excessive sun exposure or a tanning booth within 3 weeks before the start of the study
- •12. History of schistosomiasis (infection with Schistosoma parasite)
研究者
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