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临床试验/NCT02106780
NCT02106780已完成1 期

An Open Label Study to Evaluate the Pharmacokinetics of ASP1707 After a Single Oral Dose of 14C-labeled ASP1707 in Healthy Male Subjects

Astellas Pharma Europe B.V.1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2011年8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
6
试验地点
1
主要终点
Radioactivity in whole blood measured by Apparent Terminal Elimination Half-life (t1/2)

研究概览

简要总结

Subjects receive a single oral dose of radioactive ASP1707 on Day 1. Blood, plasma, urine and feces samples are collected for analysis of 14C-radioactivity and ASP1707. Metabolites are collected until at least 144 hours after dosing.

详细描述

Subjects are admitted to the clinic on Day -1 and receive a single oral dose of 14C-labeled ASP1707 on Day 1. They remain in the clinic for 6 days and are discharged on Day 7 if sufficient recovery of administered radioactivity is achieved, or the total excretion (urine + feces) per 24 hours is less than 1% of the administered dose during 2 consecutive 24-hour intervals. If these conditions are not met, the residential period may be prolonged for a maximum of 3 days. If after this time one of the conditions is still not met, subjects are requested to continue collecting their urine and/or feces at home for another 2 days. If after these additional 2 days one of the conditions is still not met, the condition of recovery of radioactivity is disregarded. Therefore only the total excretion condition is to be met by collecting 24-hour intervals for urine and feces once a week for up to 2 weeks. If the excretion condition is still not met after this time, no further samples are collected and the subject is discharged from the study.

研究设计

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

入排标准

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

入选标准

  • Subjects must be surgically sterilized and use condoms or must practice an effective contraceptive method to prevent pregnancies.
  • Body Mass Index more than or equal to 18.5 and less than 30.0 kg/m
  • Regular defecation pattern (minimum once per day).

排除标准

  • Any of the liver function tests above the upper limit of normal.
  • Exposure to radiation for diagnostic reasons (except dental X-rays and plain X-rays of thorax and bony skeleton (excluding spinal column)), during work or during participation in a clinical study in the previous year.
  • Any use of drugs of abuse within 3 months prior to admission to the Clinical Unit.
  • History of smoking more than 10 cigarettes (or equivalent amount of tobacco) per day within 3 months prior to admission to the Clinical Unit.
  • Donation of blood or blood products within 3 months prior to admission to the Clinical Unit.
  • Positive serology test for Hepatitis B Surface Antigen (HBsAg), anti Hepatitis A Virus (HAV) Immunoglobulin M (IgM), anti Hepatitis C Virus (HCV) or anti Human Immunodeficiency Virus (HIV) 1+2.

研究组 & 干预措施

1: ASP1707

Experimental

干预措施: 14C-labeled ASP1707 (Drug)

结局指标

主要结局

Radioactivity in whole blood measured by Apparent Terminal Elimination Half-life (t1/2)

时间窗: Day -1 until at least Day 7

Radioactivity in plasma measured by CL/F

时间窗: Day -1 until at least Day 7

Radioactivity in whole blood measured by Area under the plasma concentration - time curve to the last quantifiable concentration (AUClast)

时间窗: Day -1 until at least Day 7

Radioactivity in whole blood measured by Maximum concentration (Cmax)

时间窗: Day -1 until at least Day 7

Radioactivity in whole blood measured by Apparent total body clearance (CL/F)

时间窗: Day -1 until at least Day 7

Radioactivity in whole blood measured by Apparent volume of distribution (Vz/F)

时间窗: Day -1 until at least Day 7

Radioactivity in plasma measured by AUCinf

时间窗: Day -1 until at least Day 7

Radioactivity in plasma measured by AUClast

时间窗: Day -1 until at least Day 7

Radioactivity in plasma measured by Cmax

时间窗: Day -1 until at least Day 7

Radioactivity in plasma measured by tmax

时间窗: Day -1 until at least Day 7

Radioactivity in plasma measured by t1/2

时间窗: Day -1 until at least Day 7

Radioactivity in whole blood measured by Area under the plasma concentration - to time = infinity (AUCinf)

时间窗: Day -1 until at least Day 7

Radioactivity in whole blood measured by Time to Attain Cmax (tmax)

时间窗: Day -1 until at least Day 7

Radioactivity in plasma measured by Vz/F

时间窗: Day -1 until at least Day 7

Radioactivity ratio of blood / plasma concentrations per time point and of Area under the plasma concentration (AUC)

时间窗: Day -1 until at least Day 7

Excretion rate and cumulative excretion of radioactivity in urine

时间窗: Day -1 until at least Day 7

Excretion rate and cumulative excretion of radioactivity in feces

时间窗: Day -1 until at least Day 7

Total cumulative excretion of radioactivity in urine and feces

时间窗: Day -1 until at least Day 7

ASP1707 in plasma measured by AUCinf

时间窗: Day -1 until at least Day 7

ASP1707 in plasma measured by AUClast

时间窗: Day -1 until at least Day 7

ASP1707 in plasma measured by Cmax

时间窗: Day -1 until at least Day 7

ASP1707 in plasma measured by tmax

时间窗: Day -1 until at least Day 7

ASP1707 in plasma measured by t1/2

时间窗: Day -1 until at least Day 7

ASP1707 in plasma measured by CL/F

时间窗: Day -1 until at least Day 7

ASP1707 in plasma measured by Vz/F

时间窗: Day -1 until at least Day 7

ASP1707 in urine measured by Amount excreted unchanged extrapolated to time = infinity (Aeinf)

时间窗: Day -1 until at least Day 7

ASP1707 in urine measured by Amount excreted unchanged to last quantifiable sample (Aelast)

时间窗: Day -1 until at least Day 7

ASP1707 in urine measured by Renal Clearance (CLR)

时间窗: Day -1 until at least Day 7

ASP1707 in urine measured by Percentage of the dose excreted unchanged extrapolated to time = infinity (Aeinf%)

时间窗: Day -1 until at least Day 7

ASP1707 in urine measured by Percentage of the dose excreted unchanged to last quantifiable sample (Aelast %)

时间窗: Day -1 until at least Day 7

次要结局

  • Profiling of metabolites in plasma, urine and feces(Day -1 until at least Day 7)
  • Safety assessed by vital signs, 12-lead ECG, laboratory tests, adverse events, physical examination(Screening to ESV (up to Day 40))

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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