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临床试验/NCT00141180
NCT00141180已完成1 期

Placebo-Controlled, Randomized, Parallel Group, Multiple-Dose Study to Evaluate the Effects of CP-481,715 on Clinical Response and Cellular Infiltration Following Contact Allergen Challenge to the Skin of Nickel Allergic Subjects.

Pfizer6 个研究点 分布在 2 个国家目标入组 48 人开始时间: 2003年9月最近更新:
适应症
相关药物

试验速览

阶段
1 期
状态
已完成
发起方
Pfizer
入组人数
48
试验地点
6
主要终点
Effect of CP-481,715 on clinical response and cell infiltration after nickel challenge

研究概览

简要总结

To evaluate the suitability of contact allergy as a method for the evaluation of c-chemokine receptor-1 antagonist.

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

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • A history of nickel allergy confirmed by a visual positive reaction (graded at least ++) to T.R.U.E. TEST.

排除标准

  • Subjects with evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding contact allergic dermatitis or untreated, asymptomatic, seasonal allergies at time of dosing).

结局指标

主要结局

Effect of CP-481,715 on clinical response and cell infiltration after nickel challenge

次要结局

未报告次要终点

研究者

发起方
Pfizer
申办方类型
Industry

研究点 (6)

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