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临床试验/NCT01910506
NCT01910506已完成1 期

A Phase 1 Absorption, Metabolism and Excretion Study of [14C]RDEA3170 Orally Administered to Healthy Adult Male Subjects

Ardea Biosciences, Inc.0 个研究点目标入组 8 人开始时间: 2013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
8
主要终点
Characteristics of AME in terms of pharmacokinetics (PK), metabolism, and excretion

研究概览

简要总结

This study will determine the characteristics of absorption, metabolism, and excretion (AME) of RDEA3170 following a single 10 mg dose of RDEA3170 oral solution with 500 microcuries (µCi) of [14 C]RDEA3170 in healthy adult male subjects.

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
18 Years 至 55 Years(Adult)
性别
Male
接受健康志愿者

入选标准

  • Body weight ≥ 50 kg (110 lbs.) and body mass index ≥ 18 and ≤ 30 kg/m
  • No clinically relevant abnormalities in vital signs, ECG, physical examination or safety laboratory values.
  • Screening serum urate level ≤ 7.0 mg/dL.
  • Subject has a minimum of 1 bowel movement a day.

排除标准

  • History or suspicion of kidney stones.
  • History of gastrointestinal ulcers, Helicobacter pylori infection, or other disorders of gastric pH.
  • History of previous surgery on the stomach or small intestine (appendectomy is acceptable). Subject has donated blood or experienced significant blood loss (> 450 mL) within 12 weeks prior to Day 1 or has given a plasma donation within 6 weeks prior to Day
  • Inadequate venous access or unsuitable veins for repeated venipuncture.

研究组 & 干预措施

RDEA3170

Experimental

干预措施: RDEA3170 10 mg (Drug)

结局指标

主要结局

Characteristics of AME in terms of pharmacokinetics (PK), metabolism, and excretion

时间窗: Day 1 predose, 15, 30, 45 mins, 1, 1.5, 2, 2.5, 3, 4, 5, 6, 8, 10, 12, 24, 30, 36, 48, 54, 60, 72 hrs postdose (blood and plasma only); Day 1, -12 to 0, 0-6, 6-12, 12-24 hrs postdose (urine and feces only)

PK profile in terms of AUC, Tmax, Cmax, t1/2, Ae, CLr, and CL/F. AUC: area under the concentration-time curve; Tmax: time to reach maximum concentration; Cmax: maximum concentration; t1/2: apparent terminal half-life; Ae: amount of compound excreted in urine unchanged; CLr: renal clearance; CL/F: total body clearance corrected for bioavailability Metabolic profile of RDEA3170 in plasma, urine, and feces. Excretion in terms of recovery of radioactivity in urine and feces.

次要结局

  • Incidence of Adverse Events and Changes in Laboratory, Electrocardiogram, and Vital Signs Parameters(5 weeks)

研究者

申办方类型
Industry
责任方
Sponsor

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