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临床试验/NCT05127746
NCT05127746已完成1 期

An Open-label, Randomized, Cross-over, Multiple Dose, Phase 1 Clinical Trial to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of DA-5207 Transdermal Delivery System in Healthy Adults

Dong-A ST Co., Ltd.1 个研究点 分布在 1 个国家目标入组 51 人开始时间: 2021年11月25日最近更新:
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
51
试验地点
1
主要终点
AUC

研究概览

简要总结

The purpose of this study is to evaluate the safety, pharmacokinetics and pharmacodynamics of DA-5207 transdermal delivery system in healthy adults

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Health Volunteers (Age: 19~55 years)
  • Body Weight: Male≥55kg, Female≥50kg
  • 18.5 ≤BMI≤ 25.0

排除标准

  • Galactose intolerance, Lapp lactase deficiency, Glucose-galactose malabsorption
  • Allergy or Drug hypersensitivity
  • Clinically significant Medical History
  • AST, ALT>Upper Normal Range*1.25, eGFR<60mL/min/1.73m²
  • Heavy caffeine intake
  • Heavy alcohol intake (more than 210g/week)
  • Heavy smoker (more than 10 cigarettes/day)

研究组 & 干预措施

Sequence 1

Experimental

Period 1, Aricept 5mg → DA-5207 A; Period 2, Aricept 5mg → Aricept 10mg

干预措施: DA-5207 A (Drug)

Sequence 1

Experimental

Period 1, Aricept 5mg → DA-5207 A; Period 2, Aricept 5mg → Aricept 10mg

干预措施: Aricept 5mg Tablet (Drug)

Sequence 1

Experimental

Period 1, Aricept 5mg → DA-5207 A; Period 2, Aricept 5mg → Aricept 10mg

干预措施: Aricept 10mg Tablet (Drug)

Sequence 2

Experimental

Period 1, Aricept 5mg → Aricept 10mg; Period 2, Aricept 5mg → DA-5207 A

干预措施: Aricept 5mg Tablet (Drug)

Sequence 2

Experimental

Period 1, Aricept 5mg → Aricept 10mg; Period 2, Aricept 5mg → DA-5207 A

干预措施: Aricept 10mg Tablet (Drug)

Sequence 2

Experimental

Period 1, Aricept 5mg → Aricept 10mg; Period 2, Aricept 5mg → DA-5207 A

干预措施: DA-5207 A (Drug)

Sequence 3

Experimental

Period 1, Aricept 5mg → DA-5207 B; Period 2, Aricept 5mg → Aricept 10mg

干预措施: Aricept 5mg Tablet (Drug)

Sequence 3

Experimental

Period 1, Aricept 5mg → DA-5207 B; Period 2, Aricept 5mg → Aricept 10mg

干预措施: Aricept 10mg Tablet (Drug)

Sequence 3

Experimental

Period 1, Aricept 5mg → DA-5207 B; Period 2, Aricept 5mg → Aricept 10mg

干预措施: DA-5207 B (Drug)

Sequence 4

Experimental

Period 1, Aricept 5mg → Aricept 10mg; Period 2, Aricept 5mg → DA-5207 B

干预措施: Aricept 5mg Tablet (Drug)

Sequence 4

Experimental

Period 1, Aricept 5mg → Aricept 10mg; Period 2, Aricept 5mg → DA-5207 B

干预措施: Aricept 10mg Tablet (Drug)

Sequence 4

Experimental

Period 1, Aricept 5mg → Aricept 10mg; Period 2, Aricept 5mg → DA-5207 B

干预措施: DA-5207 B (Drug)

结局指标

主要结局

AUC

时间窗: 29-36 days

area under the concentration-time curve

Css,max

时间窗: 0-36 days

maximum serum concentration at steady state

次要结局

未报告次要终点

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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