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临床试验/NCT06993168
NCT06993168尚未招募1 期

An Open-label, Randomized, Single-dose, 2-sequence, 2-period, Crossover Phase 1 Study to Evaluate the Effect of Food on the Pharmacokinetic Characteristics of DA-5222 in Healthy Adult Subjects

Dong-A ST Co., Ltd.1 个研究点 分布在 1 个国家目标入组 32 人开始时间: 2025年5月21日最近更新:
干预措施
相关药物

试验速览

阶段
1 期
状态
尚未招募
入组人数
32
试验地点
1
主要终点
AUCt

研究概览

简要总结

This study is to evaluate the effect of food on pharmacokinetics of DA-5222 in healthy adult subjects

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 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy volunteers
  • BMI between 18 and 30 kg/m2
  • Body weight: Male≥50kg, Female≥45kg
  • Subjects who have signed an informed consent themselves after receiving detailed explanation about clinical study

排除标准

  • Subjects with clinically significant medical history
  • Subjects with history of drug abuse or addicted
  • Subjects with allergy or drug hypersensitivity

研究组 & 干预措施

Sequence A

Experimental

干预措施: DA-5222 (Drug)

Sequence B

Experimental

干预措施: DA-5222 (Drug)

结局指标

主要结局

AUCt

时间窗: pre-dose~72 hours post-dose

area under the curve

Cmax

时间窗: pre-dose~72 hours post-dose

maximum plasma concentration

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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