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临床试验/NCT01823900
NCT01823900已完成1 期

A Randomized, Open Label, Single-Dose, 2-Way Cross-over Clinical Trial to Compare the Safety and Pharmacokinetic Characteristics of Combination of Rosuvastatin and CS-866 and DWJ1276 in Healthy Male Volunteers

Severance Hospital1 个研究点 分布在 1 个国家目标入组 58 人开始时间: 2012年1月最近更新:
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
58
试验地点
1
主要终点
Profile of Pharmacokinetics

研究概览

简要总结

This study investigates safety and pharmacokinetic comparison of DWJ1276, a combination drug of Rosuvastatin and Olmesartan (test formulation), and co-administration of Rosuvastatin and Olmesartan (reference formulation) for single dose in healthy volunteers

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

年龄范围
20 Years 至 50 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Healthy male volunteers between the ages of 20 and 50 and within 20% of their ideal body weight, without congenital abnormality or chronic disease

排除标准

  • History of cardiovascular, pulmonary, renal, endogenous, gastrointestinal, hematologic, neurologic or hemorrhagic disease;
  • Clinically significant findings on routine laboratory (hematology, serum chemistry and urinalysis) or ECG tests;
  • Use of prescription drugs in the 14 days immediately prior to starting the study that had the potential to interact with the study medication;
  • Use of any substance that could induce or inhibit drug metabolism enzymes

研究组 & 干预措施

Test and reference formulations

Experimental

Test formulation and reference formulation given orally 7 days apart in a fasted state

干预措施: Test formulation (Drug)

Test and reference formulations

Experimental

Test formulation and reference formulation given orally 7 days apart in a fasted state

干预措施: Reference formulation (Drug)

结局指标

主要结局

Profile of Pharmacokinetics

时间窗: 0, 0.33, 0.67, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10, 12, 16, 24, 48, 72 hours post-dose

Cmax, Area Under Curve (0 to last sampling time)

次要结局

  • Profile of Pharmacokinetics(0, 0.33, 0.67, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10, 12, 16, 24, 48, 72 hours post-dose)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kyungsoo Park

Associate Professor

Severance Hospital

研究点 (1)

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