A Bioequivalence Study of Three, 2 mg Nicotine Chewing Gums (Two Tests and One Reference) in Healthy Adult Smokers
2017年12月18日 更新者:GlaxoSmithKline
A Single-Dose, Open-Label, Three-way Crossover Bioequivalence Study of Three, 2 mg Nicotine Chewing Gums (Two Tests and One Reference) in Chinese Male Healthy Adult Smokers
This is a randomized, open-label, single-dose, three-period, crossover, single-center comparative bioavailability (BA) study under fasting condition in Chinese healthy male adult participants with a history of cigarette smoking.
The participants will be admitted to the investigational clinic at least 38 hours before dosing and will remain domiciled until the completion of all study procedures at approximately 24 hours after dosing.
Three toothpastes (one is commercial non-medicated non-nicotine containing chewing gum and other two are nicotine containing gums) will be provided across the 3 treatment periods.
During each of the 3 treatment periods, participants will be under supervision in a non-smoking area and will abstain from smoking.There will be a total of at least 7 days and not more than 10 days (clinical furlough period) between treatment periods.
Twenty (20) blood samples will be collected for pharmacokinetic (PK) analysis at baseline and multiple time points following study drug administration.
The trial duration will be approximately 49 days and up to 55 days from screening to study end including the screening period.
研究概览
地位
完全的
条件
研究类型
介入性
注册 (实际的)
45
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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Beijing、中国、100032
- GSK Investigational Site
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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 45年 (成人)
接受健康志愿者
是的
有资格学习的性别
男性
描述
Inclusion Criteria:
- Participants must understand and provide written informed consent before any assessment is performed, understand the study procedures, and be willing to complete the required assessments and the study.
- Chinese male participants between 18 and 45 years of age (inclusive) in general good physical health as judged by the Investigator.
- Normal vital signs as follows:
- Oral body temperature between 35.0 and 37.5 ºC (95 and 99.5 F) inclusive
- Supine systolic blood pressure between 90 and 140 mmHg inclusive
- Supine diastolic blood pressure between 55 and 90 mmHg inclusive
- Pulse rate between 50 and 100 beats per minute (bpm) inclusive
- History of cigarette smoking of at least 10 cigarettes per day continuously for the past 3 months prior to screening.
- Body weight ≥ 50 kg, Body Mass Index (BMI) between 19 and 28 at screening.
- Ability to communicate and comply with all study requirements including the study specific chewing and swallowing procedures.
Exclusion Criteria:-
- Use of other investigational drugs within 30 days or 10 half-lives of enrollment, whichever is longer.
- History of or known hypersensitivity to the study drug or excipients.
- Diagnosis of long QT syndrome or QTc > 450 msec for males at screening.
- Any surgical or medical condition which may significantly alter the absorption, distribution, metabolism or excretion of any drug substance.
- History of malignancy or neoplastic disease of any organ system treated or untreated, orthostatic hypotension, cardiovascular disease, stroke, TIA, fainting or blackouts, clinically significant metabolic, pulmonary, neurological, hematological, autoimmune, psychiatric or endocrine disorders.. within the past 5 years prior to screening.
- Any evidence of cardiovascular, pulmonary, renal, hepatic, gastrointestinal, hematological, endocrinological, metabolic, autoimmune, neurological, psychiatric, other diseases or other clinically significant laboratory findings at screening.
- Participant has used any medication within two weeks before first scheduled study drug administration or within less than 10 times the elimination half-life of the respective drug.
- Unable to comply with the chewing and/or swallowing rhythm requirements (> 5% deviation of the total counts over 30 minutes) after trying either one of the two training sessions for 3 times.
- CO > 12 ppm after at least 38 hours confinement period in clinics prior to first dosing.
- Participants reports consumption of any drug metabolizing enzyme inducing or inhibiting aliments, evidence of current alcohol abuse or reports consumption exceeding 35 g of pure alcohol per day.
- Any history of drug hypersensitivity, asthma, urticaria, or other significant allergic diathesis, positive results in any of the virology tests for Human immunodeficiency virus (HIV)-Ab, Hepatitis C virus (HCV)-Ab, Surface antigen of the hepatitis B virus (HBs-Ag), and Tp-Ab.
- Participation in a previous clinical study with or without another investigational product and with ~470 ml blood drawn, or blood donation within the last 3 months prior to screening or previous enrollment into the current study.
- Vulnerable individual
- Inability to be venipuncture and/or tolerate venous access, unwilling to accept slight irritation of the throat and increased salivation due to nicotine gum administration.
- Unable or unwilling to discontinue the use or consumption of cigarette smoking, any nicotine containing products, Oral, local or topical pharmaceutical agents, consumption of caffeine/theophylline - containing products, grapefruit, Seville orange, orange, lemon, lime, apple, and pineapple, performance of unaccustomed strenuous physical exercise.
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:其他
- 分配:随机化
- 介入模型:交叉作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
其他:Treatment A:Treatment B:Treatment C
Participants will be administered with Treatment A(Nicorette 2 mg coated mint gum) followed by Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
其他:Treatment B:Treatment C:Treatment A
Participants will be administered with Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment A(Nicorette 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
其他:Treatment C:Treatment A:Treatment B
Participants will be administered with Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment A(Nicorette 2 mg coated mint gum) followed by Treatment B (Nicotinell 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
其他:Treatment A: Treatment C:Treatment B
Participants will be administered with Treatment A (Nicorette 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment B (Nicotinell 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
其他:Treatment B:Treatment A: Treatment C
Participants will be administered with Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment A (Nicorette 2 mg coated mint gum) followed by Treatment C (Nicotinell 2 mg coated fruit flavor gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
|
其他:Treatment C:Treatment B:Treatment A
Participants will be administered with Treatment C (Nicotinell 2 mg coated fruit flavor gum) followed by Treatment B (Nicotinell 2 mg coated mint gum) followed by Treatment A (Nicorette 2 mg coated mint gum).
Administration of each treatment will be separated by clinical furlough period of at least 7 days and not more than 10 days.
|
Participants will be administered with 2 mg coated mint gum of Nicorette
Participants will be administered with 2 mg coated mint gum of Nicotinell
Participants will be administered with 2 mg coated fruit flavor gum of Nicotinell
|
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 |
|---|---|---|
|
Area under the curve from time zero to last sampling time [AUC(0-t)]
大体时间:2 days
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AUC(0-t) will be calculated using the trapezoidal rule.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
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Area under the curve from time zero extrapolated to infinity [AUC(0-inf)]
大体时间:2 days
|
The area under the plasma concentration versus time curve will be calculated from time 0 to infinity where AUC = AUClast + Clast/λz Clast is the concentration at the last measurable sampling time point and λz is the terminal elimination rate constant.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Maximum plasma concentration (Cmax)
大体时间:2 days
|
Cmax will be obtained graphically from the plasma concentration over time profile.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Time to reach maximum plasma concentration (Tmax)
大体时间:2 days
|
Tmax will be obtained graphically from the plasma concentration over time profile.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Termination rate constant (Lambda_z)
大体时间:2 days
|
Lambda_z will be computed as the slope of the regression line of ln (C(t)) on time.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Elimination half life (t1/2)
大体时间:2 days
|
T1/2 will be computed as T1/2 = 0.693/ λz.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Systemic clearance (CL/F)
大体时间:2 days
|
CL/F will be calculated as the Dose/AUCinf, where Dose is the actual nicotine dose released.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
|
Apparent volume of distribution (Vd/F)
大体时间:2 days
|
Vd/F will be determined by the following equation: Vz/F = Dose/(lambda_z · AUCinf), where Dose is the actual nicotine dose released.
Twenty (20) blood samples will be collected at baseline and multiple timepoints following study drug administration.
|
2 days
|
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 (实际的)
2016年3月11日
初级完成 (实际的)
2016年6月12日
研究完成 (实际的)
2016年6月12日
研究注册日期
首次提交
2016年2月18日
首先提交符合 QC 标准的
2016年2月18日
首次发布 (估计)
2016年2月23日
研究记录更新
最后更新发布 (实际的)
2017年12月19日
上次提交的符合 QC 标准的更新
2017年12月18日
最后验证
2017年12月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.