Multiple Dose Study of D1971a in Healthy Volunteers
2017年4月27日 更新者:Daiichi Sankyo, Inc.
A Phase I, Double-Blind, Randomised, Placebo Controlled, Multiple-Dose Study to Assess Safety, Tolerability and Pharmacokinetics of DS-1971a in Healthy Male and Female Subjects
This is a randomised, double-blind, placebo-controlled multiple dose study designed to explore the safety, tolerability and PK of DS-1971a following oral administration over 14 days to healthy male and female subjects.
Each participant receives lidocaine as a local anaesthetic before inserting the intravenous cannula.
研究概览
详细说明
Within strictly defined limits, the protocol permits the dose escalation committee to amend the dose escalation rules, doses proposed in the study protocol and to change the timing of or to add additional assessments following review of the safety, tolerability and plasma DS-1971a concentration data.
The decisions to change the doses will be documented in the minutes of the dose escalation committee.
研究类型
介入性
注册 (实际的)
25
阶段
- 阶段1
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习地点
-
-
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London、英国
- Mammersmith Medicines Research Ltd.
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参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
18年 至 65年 (成人、年长者)
接受健康志愿者
是的
有资格学习的性别
全部
描述
Inclusion Criteria:
- Healthy male and female subjects aged 18 years to 65 years.
- A body mass index (BMI) in the range 18 kg/m2 to 30 kg/m2, inclusive, and weighing between 50 kg and 100 kg, inclusive at screening. BMI is calculated as weight [kg]/(height [m])2.
Female subjects must be of non-childbearing potential as follows:
- Must be postmenopausal (the last menstrual period was at least 12 months before Screening, and a follicle stimulating hormone [FSH] test at Screening confirms postmenopausal status); or
- Must be surgically sterile having undergone hysterectomy, bilateral oophorectomy, bilateral salpingectomy and/or bilateral tubal ligation.
- Willing to comply with all study restrictions, including the use of contraception, concomitant medication, and dietary and lifestyle restrictions.
- Sufficient intelligence to understand the nature of the study and any hazards of participating in it. Ability to communicate satisfactorily with the Investigator and to participate in, and comply with requirements of, the entire study.
- Have given written consent to participate in the study after reading the ICF, and after having the opportunity to discuss the study with the Investigator or his delegate.
- Have given written consent to have his/her data entered into The Over volunteering Prevention System.
Exclusion Criteria:
- Clinically relevant abnormal history, physical findings, ECG findings, or laboratory values that could interfere with the objectives of the study or compromise the safety of the subject.
- Presence or history of acute or chronic illness, including (but not limited to) liver or kidney disease, hypertension, seizures, or any known impairment of endocrine, or other specific body-organ dysfunction.
- History of serious reaction to any medicine.
- Presence or history of malignant disease.
- Acute or chronic infectious disease, including human immunodeficiency virus (HIV), hepatitis B virus (HBV) or C virus (HCV) infection.
- Surgery (eg, stomach bypass) or medical condition that might affect how the body handles or absorbs medicines.
- Significant illness within 4 weeks before the first dose of study medication.
- Participation in another clinical study of a new chemical entity or a prescription medicine within the previous 3 months, or unwilling to abstain from participating in other clinical trials during the study and for 3 months after receipt of study medication.
- Blood pressure (BP) and heart rate in semi-supine position at the Screening examination outside the ranges 90 mmHg to 140 mmHg systolic, 40 mmHg to 90 mmHg diastolic; heart rate < 40 beats/min to > 100 beats/min. Subjects with Stage 1 hypertension (systolic 140 mmHg to 160 mmHg; diastolic 90 mmHg to 100 mmHg) may be enrolled provided they do not have evidence of end-organ damage, diabetes or a 10 year cardiovascular risk > 20%.
- Abnormal ECG waveform morphology at Screening that would preclude accurate measurement of the uncorrected QT interval (QT) duration.
- QT interval for heart rate corrected using QTcF interval duration > 430 ms for men or > 450 ms for women, obtained as an average from the measurements on duplicate Screening ECGs over a brief recording period.
- Estimated glomerular filtration rate (eGFR) < 80 mL/min/1.73m2 (based on Modification of Diet in Renal Disease [MDRD] equation) or an absolute creatinine value outside the normal range.
- Use of any prescription or over the counter (OTC) medications, or herbal remedies (such as St John's wort), known to be strong inhibitors or strong inducers of cytochrome (CYP) enzymes (also known as CYP P450 enzymes) during the 30 days before the first dose of study medication; use of any other prescription or OTC medicine (with the exception of acetaminophen (paracetamol)), including dietary supplements or herbal remedies, during the 7 days before the dose of study medication.
- Pregnant or breastfeeding women.
- Consumption of certain foods or beverages before the first dose and throughout the study period.
- Loss of more than 400 mL blood or donation of blood, plasma, platelets, or any other blood components during the 3 months before the first dose of study medication, or unwilling to abstain from doing so during the study and for 3 months after receipt of study medication.
- Abuse of drugs or alcohol during the 2 years before the first dose of study medication, or intake of more than 21 units of alcohol weekly for male subjects and 14 units of alcohol weekly for female subjects.
- Use of tobacco products or nicotine-containing products during the 3 months before the first dose of study medication and during the study.
- Evidence of drug or alcohol abuse at screening or admission.
- Likely possibility that the volunteer will not cooperate with the requirements of the protocol.
- Objection by General Practitioner (GP) to the volunteer entering the study.
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:基础科学
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:DS-1971a (Low Dose)
Participants in Cohort 1 who receive a low dose of DS 1971a in an oral suspension
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DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
|
|
实验性的:DS-1971a (Mid dose)
Participants in Cohort 2 who receive a mid dose of DS 1971a in an oral suspension
|
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
|
|
实验性的:DS-1971a (High dose)
Participants in Cohort 3 who receive a high dose of DS 1971a in an oral suspension
|
DS 1971a is supplied as a powder or crystals and will be given as an oral suspension
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实验性的:Pooled placebo
Participants in Cohort 1, 2 or 3 who receive matching DS-1971a Placebo
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Placebo matching DS-1971a suspension
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研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of participants with at least one Treatment Emergent Adverse Event (TEAEs)
大体时间:14 days
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TEAEs are adverse events that began or got worse after treatment began.
Clinically significant changes in laboratory tests and/or physical examinations are considered adverse events.
|
14 days
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Cmax of DS-1971a
大体时间:Day 1 and Day 14
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Cmax is the highest concentration of the drug in the blood
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Day 1 and Day 14
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Tmax of DS-1971a
大体时间:Day 1 and Day 14
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Tmax is the time it takes for Cmax to be reached
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Day 1 and Day 14
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Area Under Curve at steady state (AUCtau) of DS-1971a
大体时间:Day 1 and Day 14
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AUCtau is the area under the plasma concentration-time curve at steady state.
In pharmacokinetics, steady state refers to the situation where the overall intake of a drug is about even with the rate it is being eliminated from the body.
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Day 1 and Day 14
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Area under the Curve (additional measures) for DS-1971a
大体时间:Day 1 and Day 14
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Additional AUC measures include AUC0-24 (to 24 hours), AUClast (to the last observable measure), AUC0-inf (to infinity), and AUCextr (from AUClast to infinity)
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Day 1 and Day 14
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Tmax of DS-1971a metabolites M1 and M2
大体时间:Day 1 and Day 14
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Tmax of metabolites M1 and M2 characterized by Tmax
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Day 1 and Day 14
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Cmax of DS-1971a metabolites M1 and M2
大体时间:Day 1 and Day 14
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Cmax of metabolites M1 and M2 characterized by Cmax
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Day 1 and Day 14
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AUC of DS-1971a metabolites M1 and M2
大体时间:Day 1 and Day 14
|
AUC measures include AUCtau, AUC0-24, AUClast, AUC0-inf
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Day 1 and Day 14
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始
2015年9月1日
初级完成 (实际的)
2015年12月1日
研究完成 (实际的)
2015年12月1日
研究注册日期
首次提交
2015年9月28日
首先提交符合 QC 标准的
2015年9月29日
首次发布 (估计)
2015年10月1日
研究记录更新
最后更新发布 (实际的)
2017年4月28日
上次提交的符合 QC 标准的更新
2017年4月27日
最后验证
2017年4月1日
更多信息
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