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临床试验/NCT01702181
NCT01702181已完成1 期

A Multiple-Dose (0.3%, 1%, and 3% [w/w]), Randomized, Blinded, Vehicle- and Active Comparator-Controlled, Sequential Dose Cohorts, Multi-Center Trial to Assess the Safety, Pharmacokinetics, and Proof-of-Concept Efficacy of Topical OPA 15406 Ointment, Applied Twice Daily for 28 Days, in Adult Subjects With Atopic Dermatitis

Otsuka Pharmaceutical Development & Commercialization, Inc.0 个研究点目标入组 92 人开始时间: 2012年8月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
已完成
入组人数
92
主要终点
Number of subjects with AEs, SAEs, and % of clinically relevant changes from baseline in Draize Scale, physical examinations, vital signs, laboratory assessments, and electrocardiograms.

研究概览

简要总结

The purpose of this study is to investigate the pharmacokinetics and safety of OPA-15406 in adult subjects with 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
Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult subjects 18-65 years of age
  • Diagnosis of atopic dermatitis (AD)
  • AD affecting at least 5% of total Body Surface Area (BSA) for Part 1 and at least 10% BSA for Part 2, not including face, neck, and head
  • Have had a positive but inadequate response to one or more treatment course of standard AD therapy including topical steroids, UV light A, narrowband UV B, and UV light B.

排除标准

  • Use of systemic or topical therapy for contact or atopic dermatitis within 30 days of screening

研究组 & 干预措施

Placebo

Placebo Comparator

Matching placebo.

干预措施: Placebo (Drug)

Tacrolimus

Active Comparator

Tacrolimus 0.1% ointment twice daily for 28 days.

干预措施: Tacrolimus (Drug)

OPA-15406

Experimental

干预措施: OPA-15406 (Drug)

结局指标

主要结局

Number of subjects with AEs, SAEs, and % of clinically relevant changes from baseline in Draize Scale, physical examinations, vital signs, laboratory assessments, and electrocardiograms.

时间窗: 28 days

Measurement of drug levels in the blood of treated patients

时间窗: 28 days

次要结局

  • Investigator's Global Assessment (IGA) of Disease Severity at Week 4(28 Days)

研究者

申办方类型
Industry
责任方
Sponsor

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