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临床试验/NCT01723618
NCT01723618已完成1 期

An Open-label, Randomised, Uncontrolled Trial Investigating the Pharmacokinetics of CRD007 After Single Dose Administration to Subjects With Abdominal Aortic Aneurysm (AAA)

RSPR Pharma AB1 个研究点 分布在 1 个国家目标入组 18 人开始时间: 2012年11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
18
试验地点
1
主要终点
Pharmacokinetics - maximum plasma concentration (Cmax)

研究概览

简要总结

The purpose of the study is to determine the plasma levels of CRD007 in patients with abdominal aortic aneurysms after the administration of single doses of tablets containing 10, 25 and 40 mg CRD007.

研究设计

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

入排标准

年龄范围
50 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Infra-renal abdominal aortic aneurysm

排除标准

  • Significant concurrent disease or medical conditions that are deemed to interfere with the pharmacokinetics or the safety of CRD007 conduct of the trial

研究组 & 干预措施

CRD007 10 mg

Experimental

CRD007, 10 mg tablet, single dose

干预措施: CRD007 (Drug)

CRD007 25 mg

Experimental

CRD007, 25 mg tablet, single dose

干预措施: CRD007 (Drug)

CRD007 40 mg

Experimental

CRD007, 40 mg tablet, single dose

干预措施: CRD007 (Drug)

结局指标

主要结局

Pharmacokinetics - maximum plasma concentration (Cmax)

时间窗: Pre-dose and until 12 hours post-dose

Plasma concentrations of CRD007 will be measured and standard pharmacokinetic parameters as Cmax will be measured

Pharmacokinetics - time to maximum plasma concentration (tmax)

时间窗: Pre-dose til 12 hours post-dose

Plasma concentrations of CRD007 will be measured and standard pharmacokinetic parameters as tmax will be measured.

Pharmacokinetics - Area under the plasma concentration curve (AUC)

时间窗: Pre-dose until 12 hours post-dose

Plasma concentrations of CRD007 will be measured and standard pharmacokinetic parameters as AUC will be measured.

Pharmacokinetics - elimination half life (t1/2)

时间窗: pre-dose until 12 hours post-dose

Plasma concentrations of CRD007 will be measured and standard pharmacokinetic parameters as t1/2 will be measured

次要结局

  • Dose linearity(Pre-dose and until 12 hours post-dose)
  • Potential for accumulation(Pre-dose untill 12 hours post-dose)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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