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临床试验/NCT04762407
NCT04762407已完成1 期

An Open-label, Randomized, Single-dose Crossover Study to Evaluate the Pharmacokinetics, Safety and Tolerability of HCP1903 in Healthy Subjects

Hanmi Pharmaceutical Company Limited1 个研究点 分布在 1 个国家目标入组 57 人开始时间: 2020年11月20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
发起方
入组人数
57
试验地点
1
主要终点
AUClast of Rosuvastatin

研究概览

简要总结

An open-label, randomized, single-dose crossover study to evaluate the pharmacokinetics, safety and tolerability of HCP1903 in healthy 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 45 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Age 19~45 years in healthy volunteers
  • BMI is more than 18.5 kg/m^2 , no more than 29.9 kg/m^2
  • Subjects who have ability to comprehend the objectives, contents of study and property of study drug before participating in trial and have willingness to sign of informed consent in writing

排除标准

  • Presence of medical history or a concurrent disease that may interfere with treatment and safety assessment or completion of this clinical study, including clinically significant disorders in digestive system, neuropsychiatric system, endocrine system, liver, cardiovascular system
  • Subjects who judged ineligible by the investigator

研究组 & 干预措施

Sequence 1

Experimental

Period 1 : Fasted state + HGP1910 + HGP1909, Period 2 : Fasted state + HCP1903

干预措施: HGP1910 (Drug)

Sequence 1

Experimental

Period 1 : Fasted state + HGP1910 + HGP1909, Period 2 : Fasted state + HCP1903

干预措施: HGP1909 (Drug)

Sequence 1

Experimental

Period 1 : Fasted state + HGP1910 + HGP1909, Period 2 : Fasted state + HCP1903

干预措施: HCP1903 (Drug)

Sequence 2

Experimental

Period 1 :Fasted state + HCP1903, Period 2 : Fasted state + HGP1910 + HGP1909

干预措施: HGP1910 (Drug)

Sequence 2

Experimental

Period 1 :Fasted state + HCP1903, Period 2 : Fasted state + HGP1910 + HGP1909

干预措施: HGP1909 (Drug)

Sequence 2

Experimental

Period 1 :Fasted state + HCP1903, Period 2 : Fasted state + HGP1910 + HGP1909

干预措施: HCP1903 (Drug)

结局指标

主要结局

AUClast of Rosuvastatin

时间窗: pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour

pharmacokinetic evaluation

Cmax of Free Ezetimibe

时间窗: pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour

pharmacokinetic evaluation

AUClast of Free Ezetimibe

时间窗: pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour

pharmacokinetic evaluation

Cmax of Rosuvastatin

时间窗: pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour

pharmacokinetic evaluation

次要结局

  • Cmax of Total Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • AUClast of Total Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • AUCinf of Rosuvastatin(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • Tmax of Rosuvastatin(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • t1/2 of Rosuvastatin(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • CL/F of Rosuvastatin(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • Vd/F of Rosuvastatin(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • AUCinf of Free Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • Tmax of Free Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • t1/2 of Free Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • CL/F of Free Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • Vd/F of Free Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • AUCinf of Total Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • Tmax of Total Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • t1/2 of Total Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • CL/F of Total Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)
  • Vd/F of Total Ezetimibe(pre-dose(0 hour), 0.33, 0.67, 1, 1.33, 1.67, 2, 3, 4, 5, 6, 8, 10, 12, 24, 48, 72 hour)

研究者

发起方
Hanmi Pharmaceutical Company Limited
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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