The Mass Balance Recovery, Metabolite Profile and Metabolite Identification of [14C]OD-001 in Healthy Male Participants
An Open Label, Single-Dose, Single-Period Study Designed to Assess the Mass Balance Recovery, Metabolite Profile and Metabolite Identification of [14C]OD-001 in Healthy Male Participants
This study looks at how the body handles an investigational drug called OD-001. Researchers want to learn how the medicine is absorbed, how it is broken down, and how it leaves the body.
About 8 healthy men will join the study, so that at least 6 people complete it. Each participant will drink a single dose of OD-001 as a liquid. This will be done on an empty stomach, so each participant will be asked not to eat for a period of time beforehand.
The medicine contains a small amount of a radioactive "tracer" (carbon-14). The tracer lets researchers follow the medicine and its breakdown products through your body. The amount of radioactivity is small and carefully limited. After the dose, researchers will collect samples such as blood, urine and stool. These will show how much of the medicine is recovered and what it turns into in the body.
研究概览
研究类型
注册 (估计的)
阶段
- 阶段1
联系人和位置
学习联系方式
- 姓名:Kelly Bourdon
- 电话号码:857-393-6160
- 邮箱:clinicaltrials@odysseytx.com
学习地点
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Ruddington、英国
- 招聘中
- Quotient Sciences
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接触:
- Study Coordinator
- 电话号码:+44 (0)115 974 9000
- 邮箱:clinicaltrials@odysseytx.com
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Aged 30 to 65 years inclusive at the time of signing informed consent
- Must agree to adhere to the contraception requirements. In addition, vasectomised male participants with partners of childbearing potential must have received medical assessment of the surgical success of the procedure Healthy male participants according to the assessment of the Investigator, as based on a complete medical history including a physical examination, vital signs, single 12-lead ECGs, and laboratory safety tests without any clinically significant abnormalities as measured at screening. ECGs and vital signs to be re-checked at pre-dose.
- Body mass index (BMI) of 18.0 to 35.0 kg/m2 as measured at screening.
- Must have regular bowel movements (i.e. average stool production of ≥1 and ≤3 stools per day).
Exclusion Criteria:
- Presence or history of clinically significant allergy requiring treatment, as judged by the Investigator. Hay fever is allowed unless it is active.
- History of clinically significant cardiovascular, renal, hepatic, dermatological, respiratory, particularly GI disease, especially peptic ulceration, clinically significant GI bleeding, UC, CD, Irritable Bowel Syndrome or malabsorption syndrome that may impair bioavailability, and neurological or psychiatric disorder
- Participants who are unable to take oral medication.
- Acute diarrhea, constipation or vomiting in the 7 days before the predicted Day 1. If screening occurs >7 days before Day 1his criterion will be determined on Day 1. Diarrhoea will be defined as the passage of liquid faeces and/or a stool frequency of greater than three times per day. Constipation will be defined as a failure to open the bowels more frequently than every other day
学习计划
研究是如何设计的?
设计细节
- 主要用途:其他
- 分配:不适用
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:[14C]OD-001
oral solution |
[14C]OD-001 |
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
Mass balance recovery of total radioactivity in all excreta: CumAe
大体时间:Day 1 to Day 8
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Day 1 to Day 8
|
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Mass balance recovery of total radioactivity in all excreta: Cum%Ae
大体时间:Day 1 to Day 8
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Day 1 to Day 8
|
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Number of OD-001 metabolites at ≥10% of total exposure of [14C]-radiolabel in blood
大体时间:Day 1 to Day 8
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Day 1 to Day 8
|
|
Identity of OD-001 metabolites at ≥10% of total exposure of [14C]-radiolabel in blood by LC-MS and NMR
大体时间:Day 1 to Day 8
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Day 1 to Day 8
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
Rate of elimination of [14C]OD-001 in excreta by Ae
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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Rate of elimination of [14C]OD-001 in excreta by %Ae
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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Secondary Rate of elimination of [14C]OD-001 in excreta by CumAe
大体时间:Day 1 to Day 8
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Day 1 to Day 8
|
|
Rate of elimination of [14C]OD-001 in excreta by Cum%Ae by interval
大体时间:Day 1 to Day 8
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Day 1 to Day 8
|
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Incidence of treatment-emergent adverse events
大体时间:Day 1 to Day 8
|
Day 1 to Day 8
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Percentage of [14C] total radioactivity OD-001 metabolites in excreta
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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Tmax of OD-001 in blood, total radioactivity in blood and plasma
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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Cmax of OD-001 in blood, total radioactivity in blood and plasma
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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AUC0-last of OD-001 in blood, total radioactivity in blood and plasma
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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T1/2 of OD-001 in blood, total radioactivity in blood and plasma
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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Incidence of abnormal clinical laboratory test results
大体时间:Day 1 to Day 8
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Day 1 to Day 8
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Incidence of abnormal electrocardiograms (ECGs)
大体时间:Day 1 to Day 8
|
Day 1 to Day 8
|
合作者和调查者
调查人员
- 首席研究员:Sharan Sidhu, MBChB, BAO, MRCS, MFPM、Quotient Sciences
- 研究主任:Anthony Opipari、Odyssey Therapeutics, Inc.
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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