NCT00583713已完成1 期
An Open Label Study to Assess the Effect of BLI800 on Safety and Clinical Chemistry Parameters
Braintree Laboratories0 个研究点目标入组 18 人开始时间: 2007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
- 发起方
- 入组人数
- 18
- 主要终点
- Maximum Observed Concentration (Cmax)
研究概览
简要总结
To evaluate and compare the effects on safety measures and clinical chemistry after BLI800 in two groups of patients and one group of healthy controls. The patient groups will be those with mild or moderate hepatic impairment or moderate renal disease.
研究设计
- 研究类型
- Interventional
- 分配方式
- Non Randomized
- 干预模型
- Parallel
- 主要目的
- Treatment
- 盲法
- None
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Are male or female adults who are:
- •With Child-Pugh Hepatic Dysfunction Stage A or B, or
- •With Moderate Renal Disease or
- •Healthy subjects matched to those who are enrolled in this study
- •Subjects who are considered to have only clinically non-significant conditions, as judged by the Principal Investigator and based on physical examination, laboratory profiles, medical history and ECG.
- •Female subjects who are not surgically sterile (i.e., having had a hysterectomy, bilateral oophorectomy or tubal ligation) or who are not at least 2 years naturally postmenopausal must agree to use an acceptable form of contraception.
- •Provide voluntary consent in writing to participate in this study.
排除标准
- •Subjects with known or suspected ileus, severe ulcerative colitis, gastrointestinal obstruction, gastric retention, bowel perforation, toxic colitis, or megacolon.
- •Subjects with impaired consciousness that predisposes them to pulmonary aspiration.
- •Subjects who, in the opinion of the Principal Investigator, have uncontrolled clinically significant pre-existing electrolyte disturbances, based on the Screening visit laboratory results.
- •Subjects with present or prior NYHA Functional Classification grade III or IV congestive heart failure.
- •Subjects who are pregnant or lactating, or intending to become pregnant during the study.
- •Subjects of childbearing potential who refuse a pregnancy test.
- •Subjects who have participated in an investigational clinical, surgical, drug, or device study within the past 30 days.
- •Subjects with a history of allergic or adverse response to any BLI-800 component.
- •Subjects who donated more than one pint of blood within 30 days prior to the study.
- •Subjects who donated plasma within 7 days prior to the study.
- •Subjects who had an abnormal diet or substantial changes in eating habits within 30 days prior to the start of the study.
- •Subjects who have had a bowel cleansing procedure within the past month or who have taken a laxative within the 5 days (120 hours) prior to dosing or who require a laxative every day.
- •Subjects who, in the opinion of the Investigator, should not be included in the study for any reason, including inability to follow study procedures.
研究组 & 干预措施
Renal Group
Experimental
Patients with moderate renal impairment
干预措施: BLI-800 (Drug)
Healthy volunteers
Active Comparator
Healthy volunteers
干预措施: BLI-800 (Drug)
Hepatic Group
Experimental
Patients with mild/moderate hepatic impairment.
干预措施: BLI-800 (Drug)
结局指标
主要结局
Maximum Observed Concentration (Cmax)
时间窗: 1 day
Time to Maximum Concentration
时间窗: 1 day
Terminal Half-life
时间窗: 1 day
Area Under the Curve for the 24-hour Dosing Interval
时间窗: 1 day
Elimination Rate Constant
时间窗: 1 day
次要结局
- Urinary Sulfate Concentration(pre-dose to 6 days post-dose)
研究者
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