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Clinical Study to Determine Bioequivalence Between Two Oral Medications of Empagliflozin/Metformin in 12.5 mg / 1000 mg Tablets Under Fed Conditions. (ACL24-PC020)

2026年6月8日 更新者:ADIUM

Clinical Study to Determine Bioequivalence Between Two Oral Medications of Empagliflozin/Metformin in 12.5 mg / 1000 mg Tablets in Healthy Subjects Under Fed Conditions.

Prospective, longitudinal, single-dose, randomized, open-label, crossover 2x2, two treatments, two 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 14-day wash-out period before next dosing; to compare the pharmacokinetic profile (Cmax and AUC0-t) of two 12.5/ 1000 mg empagliflozin/metformin FDC tablet in forty-two (42) healthy Mexican adult volunteers aged 18 to 55 years.

研究类型

介入性

注册 (实际的)

42

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

    • Mexico City
      • Mexico City、Mexico City、墨西哥、07870
        • Axis Clinicals Latina, S.A. de C.V.

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:

  1. Age between 18 and 55 years.
  2. Clinically healthy according to the updated medical history prior to the start of the study.
  3. Not blocked in the COFEPRIS research subject database.
  4. Body mass index between 18 and 27 kg/m².
  5. 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.
  6. Electrocardiogram (ECG) without any signs of pathology.
  7. Clinical laboratory test results within normal limits or with clinically insignificant variations.
  8. Negative biosafety tests for the presence of human immunodeficiency virus (HIV), hepatitis B virus (HBV), hepatitis C virus (HCV), and varicella-zoster virus (VDRL).
  9. Negative drug screening tests for amphetamines, benzodiazepines, cocaine, methamphetamines, morphine, and tetrahydrocannabinol (THC).
  10. Negative qualitative pregnancy test (for women).
  11. Negative breath alcohol test.
  12. Research subjects with no history of alcohol abuse or dependence, psychoactive substance abuse, or chronic medication use.
  13. Subjects with a signed informed consent form and a signed non-pregnancy commitment letter.
  14. Women who are not pregnant or breastfeeding.
  15. Women using at least one method of family planning deemed safe by the principal investigator.

Exclusion Criteria:

  1. Subjects with a history of hypersensitivity to the study drug.
  2. Subjects with lactose intolerance.
  3. 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.
  4. Subjects requiring any medication during the course of the study that interferes with the quantification or pharmacokinetics of the study drug.
  5. 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.
  6. Subjects who, prior to receiving the study drug, have taken medications such as those described in section 3.11 "Drug Interactions."
  7. 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.
  8. Subjects who have received an investigational drug within ninety days prior to the start of the study.
  9. Subjects who have donated or lost 450 mL or more of blood within sixty days prior to the start of the study.
  10. Research subjects with a history of alcohol or psychoactive substance abuse or dependence, or chronic medication use.
  11. 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.
  12. Subjects who have consumed grapefruit, cranberry, or pomegranate juice within 12 hours prior to the study.
  13. Subjects who have smoked at least 12 hours before the start of the study.
  14. Subjects who have ingested alcoholic beverages 48 hours prior to administration of the dose.
  15. Positive (qualitative) pregnancy test.

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
Synjardy 12.5/1000 mg tablet, Reference
Reference
实验性的:Test
Empagliflozin/metformin 12.5/1000 mg test
Test

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
Bioequivalence based on the pharmacokinetic parameter: Cmax
大体时间:Through 48 Hours Post Dose
Bioequivalence based on the pharmacokinetic parameter: Cmax
Through 48 Hours Post Dose
Bioequivalence based on the pharmacokinetic parameter: AUC0-t
大体时间:Through 48 Hours Post Dose
Bioequivalence based on the pharmacokinetic parameter: AUC0-t
Through 48 Hours Post Dose

次要结果测量

结果测量
措施说明
大体时间
Characterize the pharmacokinetic parameter: AUC0-inf
大体时间:Through 48 Hours Post Dose
Characterize the pharmacokinetic parameter: AUC0-inf
Through 48 Hours Post Dose
Characterize the pharmacokinetic parameter: time to maximum concentration (tmax)
大体时间:Through 48 Hours Post Dose
Characterize the pharmacokinetic parameter: time to maximum concentration (tmax)
Through 48 Hours Post Dose
Characterize the pharmacokinetic parameter: half-life (t1/2)
大体时间:Through 48 Hours Post Dose
Characterize the pharmacokinetic parameter: half-life (t1/2)
Through 48 Hours Post Dose
Establish the frequency, severity, and seriousness of adverse events that occurred during the study.
大体时间:Until the final visit (14 days after the last dose)
Establish the frequency, severity, and seriousness of adverse events that occurred during the study.
Until the final visit (14 days after the last dose)
Characterize the pharmacokinetic parameter: elimination constant (Ke)
大体时间:Through 48 Hours Post Dose
Characterize the pharmacokinetic parameter: elimination constant (Ke)
Through 48 Hours Post Dose

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

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)

2025年2月5日

初级完成 (实际的)

2025年4月4日

研究完成 (实际的)

2025年4月4日

研究注册日期

首次提交

2026年6月3日

首先提交符合 QC 标准的

2026年6月3日

首次发布 (实际的)

2026年6月8日

研究记录更新

最后更新发布 (实际的)

2026年6月10日

上次提交的符合 QC 标准的更新

2026年6月8日

最后验证

2026年6月1日

更多信息

与本研究相关的术语

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
  • 国际碳纤维联合会
  • 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.

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