Phase 1 Study in Healthy Adults to See How Sevabertinib Changes Metformin Levels in the Body
Phase 1, Open-label, Fixed-sequence Crossover Study to Investigate the Effect of Sevabertinib on the Pharmacokinetics of Metformin in Healthy Participants
研究概览
研究类型
注册 (估计的)
阶段
- 阶段1
扩展访问
联系人和位置
学习联系方式
- 姓名:Therapeutic Area Head
- 电话号码:4930300139003
- 邮箱:clinical-trials-contact@bayer.com
学习地点
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Florida
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Miami、Florida、美国、33172
- Clinical Pharmacology of Miami - Oncology
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参与标准
资格标准
适合学习的年龄
- 成人
接受健康志愿者
描述
Inclusion:
- Participant must be 18 to 55 years of age inclusive, at the time of signing the informed consent.
- Participants who are overtly healthy as determined by the investigator or medically qualified designee based on medical evaluation including medical history, physical examination, 12-lead ECG, and clinical laboratory tests.
- Participant is a non-smoker who has not used tobacco- or nicotine-containing products for at least 6 months before the first study intervention administration.
- Body mass index (BMI) within the range 18.5 to 30.0 kg/m² (inclusive) and a body weight of at least 50 kg at screening.
- Female, of non-childbearing potential only (see Section 10.4.1). Females must not be pregnant or breastfeeding, and must be documented as of non-childbearing potential (WONCBP). A negative pregnancy test is required
Exclusion:
- Existing relevant diseases of vital organs (e.g., cardiovascular, liver, gastrointestinal, renal, respiratory, or central nervous system diseases) or other organs (e.g., diabetes mellitus).
- Known history of hypersensitivity to sevabertinib, metformin, or any of their excipients.
- History of known or suspected malignant tumors.
- Regular use of medicines within 4 weeks prior to screening.
- Administration of strong or moderate inhibitors or inducers of CYP3A4, P-gp, MATE1/2-K, or OCT2 within 4 weeks or 5 half-lives prior to the first study intervention administration, whichever is longer.
- Use of any prescription drug or over-the-counter (OTC) medication within 2 weeks or 5 half-lives of the prescription medication prior to the first study intervention administration (whichever is longer), except for occasional use of acetaminophen (up to 2 g/day) within 7 days prior to the first study intervention administration.
- Use of supplements or herbal remedies within 2 weeks prior to the first study intervention administration, except for vitamins.
- Excessive intake of methylxanthine-containing drinks or food (e.g., coffee, tea, chocolate) as judged by the investigator. Excessive intake of methylxanthine is defined as the regular consumption of more than 600 mg of caffeine per day (e.g., >5 cups of coffee) or would likely be unable to refrain from the use of methylxanthine-containing beverages and food during confinement at the clinic.
- Clinically relevant findings in the ECG such as a second- or third-degree atrio-ventricular block, prolongation of the average QRS complex over 120 msec or of the QTc (Fridericia correction) interval over 450 msec or any other finding which in the opinion of the investigator will hinder participant's safety at screening or check-in (Day-1).
- Positive results for hepatitis B virus surface antigen, hepatitis B virus core antibody, hepatitis C virus antibodies, human immunodeficiency virus antibodies 1 and/or 2 at screening.
- Estimated creatinine clearance <90 mL/min according to Cockcroft-Gault formula (at screening).
- Positive urine drug and cotinine screening at screening or check-in (Day-1).
- Positive urine alcohol test at screening or check-in (Day-1).
- Unable/unwilling to comply with study restrictions.
学习计划
研究是如何设计的?
设计细节
- 主要用途:基础科学
- 分配:非随机化
- 介入模型:单组作业
- 屏蔽:无(打开标签)
武器和干预
参与者组/臂 |
干预/治疗 |
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实验性的:Metformin + Sevabertinib
Single 500 mg oral dose of metformin on Day 1 (Intervention Period 1) in healthy participants.
Sevabertinib pre-treatment period (days -4 to -1) when sevabertinib is administered alone.
Single 500 mg oral dose of metformin co-administered during ongoing sevabertinib 20 mg BID regimen on Day 1 of Intervention Period 2; sevabertinib continued on Day 2
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Immediate-release tablet, 500 mg; administered as a single 500 mg oral dose in Intervention Period 1 (Day 1) and as a single 500 mg oral dose in Intervention Period 2 (Day 1 of the combination phase, after sevabertinib pre-treatment)
Film-coated tablet, 10 mg; administered as 20 mg BID (oral) pre-treatment in Intervention Period 2 and continued 20 mg BID during co-administration with metformin
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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 |
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AUC (Area Under the Curve) of metformin
大体时间:Relative to metformin administration on Study Day 1 un until Study Day 4
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Assessed for metformin with and without sevabertinib (Metformin alone vs Metformin + sevabertinib).
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Relative to metformin administration on Study Day 1 un until Study Day 4
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AUC(0-tlast) (Area Under the Curve from time 0 to tlast) of metformin
大体时间:Relative to metformin administration on Study Day 1 un until Study Day 4
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Assessed for metformin with and without sevabertinib (Metformin alone vs Metformin + sevabertinib).
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Relative to metformin administration on Study Day 1 un until Study Day 4
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Cmax (Maximum Plasma Concentration) of metformin
大体时间:Relative to metformin administration on Study Day 1 un until Study Day 4
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Assessed for metformin with and without sevabertinib (Metformin alone vs Metformin + sevabertinib).
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Relative to metformin administration on Study Day 1 un until Study Day 4
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次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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Number of participants with treatment-emergent adverse events (TEAEs)
大体时间:From the start of study intervention until the last follow-up visit, up to 7 days after the last administration of study intervention.
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The number of participants with TEAEs will be summarized by study intervention using Medical Dictionary for Regulatory Activities (MedDRA) terms.
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From the start of study intervention until the last follow-up visit, up to 7 days after the last administration of study intervention.
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Severity of treatment-emergent adverse events (TEAEs)
大体时间:From the start of study intervention until the last follow-up visit, up to 7 days after the last administration of study intervention.
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Intensity of AEs should be documented using the National Cancer Institute’s Common Terminology Criteria for Adverse Events (NCI-CTCAE, v.5.0).
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From the start of study intervention until the last follow-up visit, up to 7 days after the last administration of study intervention.
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合作者和调查者
赞助
研究记录日期
研究主要日期
学习开始 (估计的)
初级完成 (估计的)
研究完成 (估计的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
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
- 23182
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 计划说明
Currently, there is no established plan for the sharing of Individual Patient Data (IPD) from this study. The availability of this study's data will later be determined according to Bayer's commitment to the EFPIA/PhRMA 'Principles for responsible clinical trial data sharing.' This pertains to the scope, timepoint, and process of data access.
As such, Bayer commits to considering requests from qualified researchers for patient- / study-level clinical trial data, and documents from clinical trials involving medicines and indications approved in the US and EU. However, this commitment does not reflect an active IPD sharing plan. This applies to data on new medicines and indications that have been approved by the EU and US regulatory agencies on or after January 01, 2014.
Researchers can use www.vivli.org to request access to IPD and documents from clinical studies to conduct research. Information on Bayer's criteria for listing studies is provided in the member section of the portal
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研究美国 FDA 监管的药品
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