NCT05688098已完成1 期
A Randomized, Open-label, Crossover, Phase 1 Study to Evaluate Pharmacokinetics and Safety of Irbesartan/Amlodipine High Fixed Dose Combination in Comparison With Co-administration of Mono Compounds in Healthy Volunteers
适应症
干预措施
相关药物
试验速览
- 阶段
- 1 期
- 状态
- 已完成
- 发起方
- Handok Inc.
- 入组人数
- 44
- 试验地点
- 1
- 主要终点
- AUCt of Irbesartan and Amlodipne High
研究概览
简要总结
The purpose of this study is to compare pharmacokinetics and safety of Irbesartan and Amlodipine High Fixed Dose Combination and coadministration of mono compounds in healthy adult volunteers
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Crossover
- 主要目的
- Other
- 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
- 是
入选标准
- •Patients who are 19 years or older on screening
- •Signed informed consent
- •Healthy Volunteer
- •Other inclusion applied
排除标准
- •Clinically relevant/significant findings as evaluated by the investigator
- •Other exclusion applied
研究组 & 干预措施
Irbesartan/Amlodipine High Fixed dose combination
Other
participants will receive one tablet of Irbesartan/Amlodipine High FDC in a crossover design
干预措施: Irbesartan/Amlodipine High FDC (Drug)
Co-administration of Irbesartan and Amlodipine High
Other
participants will receive one table each of Irbesartan and Amlodipine High in a crossover design
干预措施: Irbesartan (Drug)
Co-administration of Irbesartan and Amlodipine High
Other
participants will receive one table each of Irbesartan and Amlodipine High in a crossover design
干预措施: Amlodipine High (Drug)
结局指标
主要结局
AUCt of Irbesartan and Amlodipne High
时间窗: 72 hours
Cmax Irbesartan and Amlodipne High
时间窗: 72 hours
次要结局
- half-life of Irbesartan and Amlodipine High(72 hours)
- AUCinf of Irbesartan and Amlodipine High(72 hours)
- AUCt/AUCinf of Irbesartan and Amlodipine High(72 hours)
- tmax of Irbesartan and Amlodipine High(72 hours)
- CL/F of Irbesartan and Amlodipine High(72 hours)
- Vz/F of Irbesartan and Amlodipine High(72 hours)
研究者
研究点 (1)
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