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临床试验/NCT01981408
NCT01981408已完成1 期

Disposition of [^14C]-LY2801653 Following Oral Administration in Healthy Subjects

Eli Lilly and Company1 个研究点 分布在 1 个国家目标入组 6 人开始时间: 2013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
6
试验地点
1
主要终点
Urinary and Fecal Excretion of LY2801653 Radioactivity over Time expressed as a Percentage of the Total Radioactive Dose Administered

研究概览

简要总结

This type of study is called a radiolabeled study. For this study, LY2801653 (study drug) has been specially prepared to contain radiolabeled carbon [^14C]. [^14C] is a naturally occurring radioactive form of the element, carbon. This study will increase understanding about how the drug appears in the blood, urine, and stool after it is administered to healthy people. Information about any side effects that may occur will also be collected. This study will last up to 15 days for each participant, not including screening. Screening is required within 28 days prior to enrollment.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
盲法
None

入排标准

年龄范围
18 Years 至 65 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Generally healthy sterile male and female participants
  • Have a body mass index (BMI) of 18.5 to 32.0 kilograms per meter squared (kg/m^2), inclusive

排除标准

  • Regularly use known drugs of abuse and/or show positive findings on urinary drug screening
  • Have consumed herbal supplements, grapefruit juice, grapefruits, grapefruit containing products, Seville orange juice, Seville oranges, star fruit, or star fruit juice within 7 days prior to dosing or intend to consume during the study
  • Have donated blood of more than 500 milliliter (mL) within the last month
  • Have participated in a [14C]-study within the last 6 months prior to admission for this study
  • Exposure to significant radiation within 12 months prior to dose (for example, serial X-ray or computed tomography scans, barium meal, current employment in a job requiring radiation exposure monitoring)
  • Have a defecation pattern less than once per 2 days or acute constipation within 3 weeks of day before dosing

研究组 & 干预措施

[^14C]-LY2801653

Experimental

Single oral dose of LY2801653 containing 100 micro curies of radioactivity

干预措施: [^14C]-LY2801653 (Drug)

结局指标

主要结局

Urinary and Fecal Excretion of LY2801653 Radioactivity over Time expressed as a Percentage of the Total Radioactive Dose Administered

时间窗: Pre-dose up to 14 days post dose

次要结局

  • Plasma Pharmacokinetics of LY2801653 and Radioactivity Maximum Observed Concentration (Cmax)(Pre-dose up to 14 days post dose)
  • Plasma Pharmacokinetics of LY2801653 and Radioactivity Time of Maximum Concentration (tmax)(Pre-dose up to 14 days post dose)
  • Plasma Pharmacokinetics of LY2801653 and Radioactivity Area Under The Concentration-time Curve from zero to the last timepoint with a measurable Concentration (AUC 0 to tlast)(Pre-dose up to 14 days post dose)
  • Relative Abundance of LY2801653 and the Metabolites of LY2801653 in Urine and Feces(Pre-dose up to 14 days post dose)
  • Relative Abundance of LY2801653 and the Metabolites of LY2801653 in Plasma(Pre-dose up to 14 days post dose)

研究者

申办方类型
Industry
责任方
Sponsor

研究点 (1)

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