Clinical Study to Determine Bioequivalence of Oral Tamsulosin Products as 0.4 mg Prolonged-release Tablets in Male Subjects Under Fed Conditions (ACL25-PC007)
2026年7月7日 更新者:ADIUM
Clinical Study to Determine Bioequivalence Between Two Oral Tamsulosin Products as 0.4 mg Prolonged-release Tablets in Healthy Male Subjects Under Fed Conditions
Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x4, replicated, two treatments, four periods, two sequences controlled clinical study
研究概览
详细说明
The study design was a randomized, open-label, two-way, crossover, single-dose, prospective, and longitudinal study, with a 7-day wash-out period before next dosing; to compare the pharmacokinetic profile (Cmax, AUC0-t and AUC0-inf) of two 0.4 mg tamsulosin extended release tablet in sixty-six (66) healthy male Mexican adult volunteers aged 18 to 55 years.
研究类型
介入性
注册 (实际的)
66
阶段
- 不适用
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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Mexico City
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Mexico City、Mexico City、墨西哥、07870
- Axis Clinicals Latina, S.A. de C.V.
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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
- 成人
接受健康志愿者
是的
描述
"Inclusion Criteria:
- Age between 18 and 55 years.
- Clinically healthy male according to the updated medical history prior to the start of the study.
- Not blocked in the COFEPRIS research subject database.
- Body mass index between 18 and 27 kg/m².
- Normal vital signs: Heart rate between 60 and 99 beats per minute, respiratory rate between 12 and 20 breaths per minute, systolic blood pressure between 90-130 mmHg, diastolic blood pressure between 60-89 mmHg, and temperature between 36.0 and 37.4°C.
- Electrocardiogram (ECG) without any signs of pathology.
- Clinical laboratory test results within normal limits or with clinically insignificant variations.
- Negative biosafety tests for the presence of human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), and varicella-zoster virus (VDRL).
- Negative drug screening tests for amphetamines, benzodiazepines, cocaine, methamphetamines, morphine, and tetrahydrocannabinol (THC).
- Negative breath alcohol test.
- Research subjects with no history of alcohol abuse or dependence, psychoactive substance abuse, or chronic medication use.
- Subjects with a signed informed consent form.
Exclusion Criteria:
- Subjects with a history of hypersensitivity to the study drug.
- Subjects with lactose intolerance.
- Subjects with a history of cardiovascular, renal, hepatic, metabolic, gastrointestinal, neurological, endocrine, hematopoietic (any type of anemia), mental illness, or other organic abnormalities that could affect the pharmacokinetic study of the study product.
- Subjects requiring any medication during the course of the study that interferes with the quantification or pharmacokinetics of the study drug.
- Subjects who have been exposed to agents known to induce or inhibit hepatic enzyme systems or who have taken potentially toxic medications within 30 days prior to the start of the study.
- Subjects who, prior to receiving the study drug, have taken medications such as those described in section 3.11 "Drug Interactions."
- Subjects who have been hospitalized for any reason within sixty days prior to the start of the study or who have been seriously ill within thirty days prior to the start of the study.
- Subjects who have received an investigational drug within ninety days prior to the start of the study.
- Subjects who have donated or lost 450 mL or more of blood within sixty days prior to the start of the study.
- Research subjects with a history of alcohol or psychoactive substance abuse or dependence, or chronic medication use.
- Subjects who have consumed beverages or foods containing xanthines (coffee, tea, cocoa, chocolate, yerba mate, cola, etc.) or have consumed charcoal-grilled foods within 12 hours prior to administration of the medication dose.
- Subjects who have consumed grapefruit, cranberry, or pomegranate juice within 12 hours prior to the study.
- Subjects who have smoked at least 12 hours before the start of the study.
- Subjects who have ingested alcoholic beverages 48 hours prior to administration of the dose."
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:卫生服务研究
- 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 |
|---|---|
|
有源比较器:Reference
Omnic Ocas, 0.4 mg, ER tablet, Reference
|
TEST
REFERENCE
|
|
实验性的:Test
Tamsulosin 0.4 mg ER tablet, test
|
TEST
REFERENCE
|
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 |
|---|---|---|
|
基于药代动力学参数Cmax的生物等效性
大体时间:给药后72小时内
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基于药代动力学参数Cmax的生物等效性
|
给药后72小时内
|
|
Bioequivalence based on the pharmacokinetic parameter: AUC0-t
大体时间:Through 72 hours Post Dos
|
Bioequivalence based on the pharmacokinetic parameter: AUC0-t
|
Through 72 hours Post Dos
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
表征药代动力学参数:AUC0-inf
大体时间:给药后72小时内
|
描述药代动力学参数:AUC0-inf
|
给药后72小时内
|
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表征药代动力学参数:达峰时间(tmax)
大体时间:给药后72小时内
|
描述药代动力学参数:达峰时间(tmax)
|
给药后72小时内
|
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表征药代动力学参数:消除常数(Ke)
大体时间:给药后72小时内
|
表征药代动力学参数:消除常数(Ke)
|
给药后72小时内
|
|
描述药代动力学参数:半衰期 (t1/2)
大体时间:给药后72小时内
|
表征药代动力学参数:半衰期(t1/2)
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给药后72小时内
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确定研究期间发生的不良事件的频率、严重程度和严重性。
大体时间:直至末次访视(末次给药后7天)
|
确定研究期间发生的不良事件的频率、严重程度和严重性。
|
直至末次访视(末次给药后7天)
|
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。
赞助
出版物和有用的链接
负责输入研究信息的人员自愿提供这些出版物。这些可能与研究有关。
一般刊物
- Accennato VAC, Costa F, Riccio MF, Bernasconi G, Noboli AC. Bioequivalence Between Two Fixed Dose Combinations of Dutasteride and Tamsulosin in Male Subjects Under Fasting and Fed Conditions. Int Ann Med. 2017;1(10).
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)
2026年2月12日
初级完成 (实际的)
2026年4月16日
研究完成 (实际的)
2026年4月16日
研究注册日期
首次提交
2026年7月7日
首先提交符合 QC 标准的
2026年7月7日
首次发布 (实际的)
2026年7月13日
研究记录更新
最后更新发布 (实际的)
2026年7月13日
上次提交的符合 QC 标准的更新
2026年7月7日
最后验证
2026年7月1日
更多信息
与本研究相关的术语
其他研究编号
- ACL25-PC007
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
是的
IPD 计划说明
Upon request, the clinical research site will provide this data with prior authorization from the sponsor, without disclosing personal information.
All information will be uniquely identified by the research subject's initials and/or their assigned randomization number, thus guaranteeing their privacy.
IPD 共享时间框架
Upon request
IPD 共享访问标准
Upon request
IPD 共享支持信息类型
- 研究方案
- 企业社会责任
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.