NCT03289208已完成1 期
An Open-Label, Single-Dose Study to Evaluate the Pharmacokinetics of MCI-186 in Subjects With Mild or Moderate Renal Impairment Compared to Subjects With Normal Renal Function
Shionogi1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2016年10月27日最近更新:
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
- 30
- 试验地点
- 1
- 主要终点
- AUC0-last
研究概览
简要总结
To assess the pharmacokinetics of MCI-186 after a single intravenous infusion of 30mg/hour in subjects with mild or moderate renal impairment compared to subjects with normal renal function.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Other
- 盲法
- None
入排标准
- 年龄范围
- 20 Years 至 75 Years（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •All subjects
- •Able to provide written informed consent to participate in this study after reading the ICF
- •Subjects is able to understand and willing to cooperate and comply with the Protocol restrictions and requirements
- •A body weight of ≥45 kg in males or ≥40 kg in females and a body mass index ranging from 18 to 30 kg/m2
- •Renal impaired subjects (in addition)
- •Subjects with mild renal impairment defined as eGFR 60-89 mL/min/1.73m2 and subjects with moderate renal impairment defined as eGFR 30-59 mL/min/1.73m2
- •Chronic and stable renal impairment
- •Healthy subjects (in addition)
- •Subject with normal renal function defined as eGFR≥90 mL/min/1.73m2
- •Good health and free from clinically significant illness or disease
排除标准
- •All subjects
- •Presence or history of severe allergy to food, or any medicinal product or relevant excipient that is of clinical significance
- •Subjects were previously administered MCI-186
- •Positive urine drug screen (if not due to concomitant medication) or alcohol test
- •History of alcohol abuse or drug abuse
- •Presence of active infection requiring antibiotics
- •Positive test for human immunodeficiency virus (HIV) antigen/antibody, hepatitis B surface antigen (HBsAg), or hepatitis C virus antibody (HCVAb)
- •Renal impairment subject (in addition)
- •Acute renal failure
- •History of renal transplantation
- •Aspartate aminotransferase (AST) activity, or an alanine aminotransferase (ALT) activity of at least 3 times the upper limit of normal (ULN) range
- •Uncontrolled, or untreated hypertension defined as systolic blood pressure (SBP)>180 mmHg and/or diastolic blood pressure (DBP)>110 mmHg
- •Start of any new medication or new any changes to a current dosage
- •Healthy subject (in addition)
- •History or presence of any renal disease
- •Uncontrolled, or untreated hypertension defined as systolic blood pressure (SBP)>160 mmHg and/or diastolic blood pressure (DBP)>100 mmHg
研究组 & 干预措施
mild renal impairment
Experimental
干预措施: MCI-186 (Drug)
moderated renal impairment
Experimental
干预措施: MCI-186 (Drug)
normal renal function
Experimental
干预措施: MCI-186 (Drug)
结局指标
主要结局
AUC0-last
时间窗: pre-dose, 0.25h, 0.5h, 1h, 1.5h, 2h, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h and 48h post-dose
Cmax
时间窗: pre-dose, 0.25h, 0.5h, 1h, 1.5h, 2h, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h and 48h post-dose
AUC0-∞
时间窗: pre-dose, 0.25h, 0.5h, 1h, 1.5h, 2h, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h and 48h post-dose
次要结局
- t½(pre-dose, 0.25h, 0.5h, 1h, 1.5h, 2h, 3h, 4h, 6h, 8h, 10h, 12h, 24h, 36h and 48h post-dose)
研究者
研究点 (1)
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