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临床试验/NCT01429688
NCT01429688已完成1 期

A Randomized, Single-dose, 2-sequence, 2-period Crossover Study to Investigate the Food-effect Pharmacokinetics of Sarpogrelate HCl Controlled Release Tablet in Healthy Male Subjects

Alvogen Korea1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2011年7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
发起方
入组人数
36
试验地点
1
主要终点
Composite of pharmacokinetics

研究概览

简要总结

The purpose of this study is compare the safety and pharmacokinetic characteristics of DP-R202 (Sarpogrelate HCl 100mg, qd) with those of Anplag (Sarpogrelate HCl 100mg, tid) after multiple oral administration in healthy male volunteers.

详细描述

The number of patient is thirthy-six.Patients were randomly assigned either anplag tablet(Sarpogrelate HCL 100mg, tid)3days first, DP-R202(Sarpogrelate HCL 300mg, qd) 3days Second or DP-R202(Sarpogrelate HCL 300mg, qd)3days first, anplag tablet(Sarpogrelate HCL 100mg, tid) 3days second.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
盲法
None

入排标准

年龄范围
20 Years 至 55 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • 20 to 55 years of healthy volunteers

排除标准

  • Hypersensitivity Reaction about Sarpogrelate HCL or other antiplatelets

研究组 & 干预措施

DP-R202

Experimental

Multiple oral administration for 3 days

干预措施: Anplag (Drug)

Anplag

Active Comparator

Multiple oral administration for 3days

干预措施: Anplag (Drug)

结局指标

主要结局

Composite of pharmacokinetics

时间窗: comparator 0, 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 6.33, 6.67, 7, 7.5, 8, 9, 12, 12.33, 12.67, 13, 13.5, 14, 15, 16, 24h Test drug : 0, 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 5, 6, 8, 12, 16, 24h

Cmax, ss, AUCτ

次要结局

  • Composite of pharmacokinetics(comparator 0, 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 6, 6.33, 6.67, 7, 7.5, 8, 9, 12, 12.33, 12.67, 13, 13.5, 14, 15, 16, 24h Test drug : 0, 0.25, 0.5, 0.75, 1, 1.5, 2, 3, 4, 5, 6, 8, 12, 16, 24h)

研究者

发起方
Alvogen Korea
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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