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临床试验/NCT03005223
NCT03005223Unknown1 期

Drug-Drug Interaction Study Between DWC20155 / DWC20156 and DWC20163 in Healthy Volunteers

Daewoong Pharmaceutical Co. LTD.0 个研究点目标入组 52 人开始时间: 2017年1月4日最近更新:
适应症
干预措施

试验速览

阶段
1 期
发起方
入组人数
52
主要终点
Maximum Plasma Concentration (Cmax)

研究概览

简要总结

A randomized, open label, crossover study to explore drug-drug interactions between DWC20155 / DWC20156 and DWC20163 in Healthy Volunteers

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 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Accepts healthy volunteers

排除标准

  • Who has allergy to investigational product

研究组 & 干预措施

Study effect of DWC20163 on DWC20155/DWC20156 PK

Experimental

To study effect of DWC20163 on DWC20155/DWC20156 PK

干预措施: Co-administration of DWC20155/DWC20156 (Drug)

Study effect of DWC20163 on DWC20155/DWC20156 PK

Experimental

To study effect of DWC20163 on DWC20155/DWC20156 PK

干预措施: DWC20163 (Drug)

Study effect of DWC20155/DWC20156 on DWC20163 PK

Experimental

To study effect of DWC20155/DWC20156 on DWC20163 PK

干预措施: Co-administration of DWC20155/DWC20156 (Drug)

Study effect of DWC20155/DWC20156 on DWC20163 PK

Experimental

To study effect of DWC20155/DWC20156 on DWC20163 PK

干预措施: DWC20163 (Drug)

结局指标

主要结局

Maximum Plasma Concentration (Cmax)

时间窗: 0 ~ 24 hours

Area under the time versus plasma concentration curve (AUC)

时间窗: 0 ~ 24 hours

次要结局

未报告次要终点

研究者

发起方
Daewoong Pharmaceutical Co. LTD.
申办方类型
Industry
责任方
Sponsor

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