A Bioequivalence Study Between Telmione Plus 80/12.5mg and Micardis Plus 80/12.5 mg in Healthy Adult Volunteers
2022年2月14日 更新者:HK inno.N Corporation
A Bioequivalence Study to Compare and Evaluate the Pharmacokinetic Characteristics and the Safety After Administration of TELMIONE PLUS TAB. 80/12.5mg and MICARDIS PLUS TAB. 80/12.5mg in Healthy Adult Volunteers
To compare the pharmacokinetics and safety after a single dose administration of Telmione plus® 80/12.5mg
and Micardis plus® 80/12.5mg in healthy adult volunteers
研究概览
研究类型
介入性
注册 (实际的)
46
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
-
-
Chungcheongbuk-do
-
Cheongju-si、Chungcheongbuk-do、大韩民国、28644
- Chungbuk National University Hospital
-
-
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
19年 及以上 (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 adult volunteers aged ≥ 19 years at screening
- Body weight ≥ 50kg and Body mass index (BMI) in the range of 18.0 and 30.0 kg/㎡
- Subjects who do not have congenital or chronic diseases requiring treatment and have no pathological symptoms or findings as a result of physical examination
- Determined by the investigator to be eligible for study participation based on the results of screening tests (clinical laboratory tests, vital signs, physical examination, 12-lead ECG) conducted according to the IP characteristics
- Subjects who decided to participate in the study and signed informed consent form voluntarily after receiving detailed explanation of the study and fully understanding
Exclusion Criteria:
- Subjects with a presence and a history of clinically significant hepatic, renal, neurology, psychiatric, pulmonary, endocrine, hematologic, oncologic, genitourinary, cardiovascular, gastrointestinal, musculoskeletal disease
- Pregnant(positive urine HCG) or breastfeeding women if female
- Subjects with a hereditary problems, for example, galactose intolerance, Lapp lactase deficiency or glucose-galactose malabsorption
- Subjects with a presence and a history of surgery or gastrointestinal diseases which might significantly change absorption of medicines
- Subjects with hypersensitivity or a history of clinically significant hyper sensitivity to ingredients with IPs, excipients, other drugs including sulfonamide and renin-angiotensin class
Subjects with the following results in clinical laboratory tests
- AST/ALT/ALP/γ-GTP/Bilirubin total > UNL (upper normal limit) × 2
- Creatinine in plasma which is outside the accepted normal range or eGFR calculated by MDRD < 60 mL/min/1.73 ㎡
- CK > UNL × 2
- Subjects with a history of drug abuse or positive to drug abuse at urine drug screening test
- Subjects with systolic blood pressure (SBP) ≥ 140 mmHg or ≤ 90 mmHg, diastolic blood pressure (DBP) ≥ 100 mmHg or ≤ 60 mmHg, or pulse rate (PR) ≤ 40 bpm or ≥ 100 bpm on vital signs measured in sitting position after taking a rest for at least 3 minutes during screening test
Subjects with clinically significant opinions including the following results in 12-lead ECG test during screening test
- QTc > 450 ms
- PR interval > 200 ms
- QRS duration > 120 ms
- Subjects who have an abnormal diet that can affect ADME of drugs or consume foods that can affect drug metabolism
- Subjects who have taken any prescription drugs or herbal medicine within 2 weeks prior to the 1st IP administration, or any over-the-counter (OTC) drug, health functional food or vitamin preparation within 10 days to the 1st IP administration (However, can participate in the study if otherwise eligible in the judgment of the investigator)
- Subjects who have taken the drug which can induce or inhibit drug metabolism enzyme within 1 month prior to the 1st IP administration
- Subjects who have participated in any other clinical study or bioequivalnece study within 6 months prior to the 1st IP administration(However, the criterion for termination of participation in other clinical study or bioequivalence study is the last administration date, and the next day is counted as one day.)
- Subjects who have donated whole blood within 2 months prior to the 1st IP administration or have donated blood components or received transfusion within 1 month prior to the 1st IP administration
Subject who have continued drink of alcohol (> 21 units/week, 1 unit = 10 g = 12.5 mL of pure alcohol) within 6 months prior to the 1st IP administration or are unable to stop drinking from the time of signing the informed consent form to post study visit
- alcohol (g) = intake volume(mL) × level(%) × 0.8
- Subject who have a history of excessive smoking (> 10 cigarettes/day) within 3 months prior to the 1st IP administration and unable to stop smoking from 24 hours before the administration at each period to the last sampling time at each period
- Subjects who take or are unable to stop foods containing grapefruit from 48 hours before the 1st IP administration to post study visit
- Subject who take or are unable to stop foods containing caffeine(coffee, green tea, black tee, soda, coffee-flavored milk, nutritive tonic drink) from 24 hours before the administration at each period to the last sampling time at each period
- Subjects who have exercised vigorously exceeding the level of daily life during the period from 48 hours before the 1st administration to post study visit, or who are unable to stop vigorous exercise
- Subjects or their spouse or partner who are not using an approved method of contraception or even if are not planning to become pregnant (e.g., contraceptive administration and implantation, intrauterine device, Those who are not using procedures (vasectomy, tubal ligation, etc.) from the time of written consent of the subject until two weeks after the last bioequivalence study drug administration date
- Subjects who have determined that the investigator is unsuitable to participate in the bioequivalence test due to reasons other than the above selection/exclusion criteria
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:治疗
- 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 |
|---|---|
|
实验性的:序列A
TRTR
|
Test drug (Fixed-dose combination drug of telmisartan 80mg and hydrochlorothiazide 12.5mg)
Reference drug (Fixed-dose combination drug of telmisartan 80mg and hydrochlorothiazide 12.5mg)
|
|
实验性的:序列B
RTRT
|
Test drug (Fixed-dose combination drug of telmisartan 80mg and hydrochlorothiazide 12.5mg)
Reference drug (Fixed-dose combination drug of telmisartan 80mg and hydrochlorothiazide 12.5mg)
|
研究衡量的是什么?
主要结果指标
结果测量 |
大体时间 |
|---|---|
|
替米沙坦的Cmax
大体时间:长达 72 小时
|
长达 72 小时
|
|
AUClast 替米沙坦
大体时间:长达 72 小时
|
长达 72 小时
|
|
Cmax of hydrochlorothiazide
大体时间:Up to 72 hours
|
Up to 72 hours
|
|
AUClast of hydrochlorothiazide
大体时间:Up to 72 hours
|
Up to 72 hours
|
次要结果测量
结果测量 |
大体时间 |
|---|---|
|
替米沙坦的Tmax
大体时间:长达 72 小时
|
长达 72 小时
|
|
替米沙坦的 AUCinf
大体时间:长达 72 小时
|
长达 72 小时
|
|
替米沙坦的 t1/2
大体时间:长达 72 小时
|
长达 72 小时
|
|
替米沙坦的 CL/F
大体时间:长达 72 小时
|
长达 72 小时
|
|
替米沙坦的Vd/F
大体时间:长达 72 小时
|
长达 72 小时
|
|
Tmax of hydrochlorothiazide
大体时间:Up to 72 hours
|
Up to 72 hours
|
|
AUCinf of hydrochlorothiazide
大体时间:Up to 72 hours
|
Up to 72 hours
|
|
t1/2 of hydrochlorothiazide
大体时间:Up to 72 hours
|
Up to 72 hours
|
|
CL/F of hydrochlorothiazide
大体时间:Up to 72 hours
|
Up to 72 hours
|
|
Vd/F of hydrochlorothiazide
大体时间:Up to 72 hours
|
Up to 72 hours
|
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)
2021年7月8日
初级完成 (实际的)
2021年10月31日
研究完成 (实际的)
2021年10月31日
研究注册日期
首次提交
2021年8月25日
首先提交符合 QC 标准的
2021年9月1日
首次发布 (实际的)
2021年9月10日
研究记录更新
最后更新发布 (实际的)
2022年2月16日
上次提交的符合 QC 标准的更新
2022年2月14日
最后验证
2022年2月1日
更多信息
与本研究相关的术语
其他相关的 MeSH 术语
其他研究编号
- IN_TMP_101
药物和器械信息、研究文件
研究美国 FDA 监管的药品
不
研究美国 FDA 监管的设备产品
不
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.