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A Clinical Trial to Assess the Pharmacokinetic Profile of Propylene Glycol (PG) in Healthy Adults Following PG Exposure

2026年7月6日 更新者:American Beverage Association

An Open-label, Dose-escalation Clinical Trial to Assess the Pharmacokinetic Profile of Propylene Glycol (PG) in Healthy Adults Following PG Exposure

The goal of this clinical trial is to determine the translation of propylene glycol (PG) exposure in beverages to circulating PG levels to better understand the margin of safety in healthy participants. The main question it aims to answer is what is the maximum concentration (Cmax) of propylene glycol (PG) in serum following consumption of one, two, or three PG-containing beverages? Participants will be asked to:

  • Consume 1x, 2x, and 3x 12oz of PG-containing beverage
  • Have their blood drawn
  • Complete urine pregnancy testing if of childbearing potential
  • Complete a study diary and record their food and beverage consumption
  • Have their vital signs and oxygen measurements taken

研究概览

研究类型

介入性

注册 (估计的)

30

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。

学习联系方式

学习地点

    • Ontario
      • London、Ontario、加拿大、N5Y 5V6
        • 招聘中
        • KGK Science Inc.

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
  • 年长者

接受健康志愿者

是的

描述

Inclusion Criteria:

  1. Males and females 18 years and older
  2. Body Mass Index (BMI) between 18.5 to 29.9 kg/m2
  3. Females not of child-bearing potential, defined as those who have undergone a sterilization procedure (e.g. hysterectomy, bilateral oophorectomy, bilateral tubal ligation, complete endometrial ablation) or have been post-menopausal for at least 1 year prior to screening Or,

    Individuals of child-bearing potential must have a negative baseline urine pregnancy test and agree to use a medically approved method of birth control for the duration of the study. All hormonal birth control must have been in use for a minimum of three months. Acceptable methods of birth control include:

    • Hormonal contraceptives including oral contraceptives, hormone birth control patch (Ortho Evra), vaginal contraceptive ring (NuvaRing), injectable contraceptives (Depo-Provera, Lunelle), or hormone implant (Nexplanon)
    • Double-barrier method
    • Intrauterine devices
    • Non-heterosexual lifestyle and agrees to use contraception if planning on changing to heterosexual partner(s)
    • Vasectomy of partner at least 6 months prior to screening
    • Abstinence and agrees to use contraception if planning on becoming sexually active during the study
  4. Agrees to refrain from vigorous physical activity and alcohol consumption 24 hours prior to dosing day (i.e., Day 1 of each study period which corresponds to Visits 2, 4, 6) and Day 2 of each study period
  5. Willingness to complete diaries, food records, and to complete all clinic visits
  6. Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study
  7. Provided voluntary, written, informed consent to participate in the study
  8. Healthy as determined by medical history and laboratory results as assessed by the Qualified Investigator (QI)

Exclusion Criteria:

  1. Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
  2. Allergy, sensitivity, or intolerance, preventing consumption of investigational product ingredients and standardized meal
  3. Individuals with alcohol dehydrogenase deficiency as assessed by the QI
  4. Poor venous access as assessed by the QI
  5. History of or current diagnosis with kidney and/or liver diseases as assessed by the QI on a case-by case basis, with the exception of history of kidney stones in participants who are symptom free for 6 months
  6. Significant cardiovascular event in the past 6 months. (Participants with no significant cardiovascular event on stable medication may be included after assessment by the QI on a case-by-case basis.)
  7. Self-reported confirmation of any significant neuropsychological condition (e.g., Schizophrenia, bipolar disorder, post-traumatic stress disorder, brain injury, neurodegenerative disease, infections, insomnia, anxiety, depression, epileptic or other seizure-related disorders) as assessed by the QI
  8. Unstable metabolic disease or chronic diseases as assessed by the QI
  9. Current or history of any significant diseases of the gastrointestinal tract as assessed by the QI
  10. Unstable hypertension. Treatment on a stable dose of medication for at least 3 months will be considered by the QI (See Section 7.3)
  11. Self-reported confirmation of current or pre-existing thyroid condition. Treatment on a stable dose of medication for at least 3 months will be considered by the QI
  12. Major surgery in the past 3 months or individuals who have planned surgery during the course of the study. (Participants with minor surgery will be considered on a case-by-case basis by the QI.)
  13. Cancer, except skin basal cell carcinoma completely excised with no chemotherapy or radiation with a follow up that is negative. Volunteers with cancer in full remission for more than five years after diagnosis are acceptable.
  14. Individuals with an autoimmune disease or are immune compromised as assessed by the QI.
  15. Self-reported confirmation of a HIV-, Hepatitis B- and/or C-positive diagnosis as assessed by the QI
  16. Self-reported confirmation of blood/bleeding disorders as assessed by the QI
  17. Use of prescribed cannabinoid products
  18. Chronic use of cannabinoid products (>2 times/week). Occasional users will be required to washout and abstain for the duration of the study period
  19. Regular use of e-cigarettes, tobacco or nicotine products in the past six months, as assessed by the QI. Occasional users will be required to washout (1 month) and abstain for the duration of the study period.
  20. Alcohol intake average of >1 standard drinks per day as assessed by the QI
  21. Alcohol or drug abuse within the last 12 months
  22. Current use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the safety of the investigational product (Sections 7.3.1 and 7.3.2)
  23. Clinically significant abnormal laboratory results at screening as assessed by the QI
  24. Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
  25. Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
  26. Individuals who are unable to give informed consent
  27. Any other condition or lifestyle factor, that, in the opinion of the QI, may adversely affect the participant's ability to complete the study or its measures or pose significant risk to the participant

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:基础科学
  • 分配:不适用
  • 介入模型:顺序分配
  • 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:Propylene glycol-containing beverage
Participants will consume a beverage containing propylene glycol (PG) with standardized meals at Visits 2, 4, and 6.
At Visits 2, 4, and 6, participants will consume 1X, 2X, and 3X 12 oz of a PG-containing beverage (in bottle format) with standardized meals in the presence of the study staff over the course of the dosing day. Participants will consume the beverage and standardized meal within 15 minutes. The only beverage allowed during the visit - other than the intent-to-treat beverage - will be water.

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
The maximum concentration of propylene glycol in serum
大体时间:From pre-dose through 24 hours post-dose.
The maximum concentration (Cmax) of propylene glycol (PG) in serum following consumption of one, two, or three PG-containing beverages.
From pre-dose through 24 hours post-dose.

次要结果测量

结果测量
措施说明
大体时间
Serum PG Levels
大体时间:Baseline (pre-dose) at each dosing visit
The difference in baseline serum PG levels between each study period.
Baseline (pre-dose) at each dosing visit
Tmax
大体时间:From pre-dose through 24 hours post-dose
Assessment of Tmax for PG following consumption of one, two, or three PG containing beverages.
From pre-dose through 24 hours post-dose
Area Under the Curve (AUC0-24hrs)
大体时间:From pre-dose through 24 hours post-dose
Assessment of Area Under the Curve (AUC0-24hrs) for PG following consumption of one, two, or three PG containing beverages.
From pre-dose through 24 hours post-dose
AUC0-∞
大体时间:From pre-dose through 24 hours post-dose
Assessment of AUC0-∞ for PG following consumption of one, two, or three PG containing beverages.
From pre-dose through 24 hours post-dose
Terminal elimination half-life (t1/2)
大体时间:From pre-dose through 24 hours post-dose
Assessment of terminal elimination half-life (t1/2) for PG following consumption of one, two, or three PG containing beverages.
From pre-dose through 24 hours post-dose
Measured and calculated osmolality
大体时间:Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose
Analysis of osmolality at baseline (0 hour) and at each timepoint (0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, 24 hours) following consumption of one, two, or three PG containing beverages. Calculated osmolality will be derived from serum sodium, urea, and glucose concentrations.
Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose
Blood osmolal gap
大体时间:Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose
Analysis of blood osmolal gap at baseline (0 hour) and at each timepoint (0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, 24 hours) following consumption of one, two, or three PG containing beverages.
Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose
Serum lactate concentration
大体时间:Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose
Analysis of serum lactate concentrations at baseline (0 hour) and at each timepoint (0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, 24 hours) following consumption of one, two, or three PG containing beverages.
Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose
pyruvate concentration
大体时间:Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose
Analysis of pyruvate concentrations at baseline (0 hour) and at each timepoint (0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, 24 hours) following consumption of one, two, or three PG containing beverages.
Assessed at baseline (0 hour) and at 0.5 hour, 1 hour, 1.5 hours, 2 hours, 4 hours, 5 hours, 6 hours, 8 hours, 9 hours, 12 hours, and 24 hours post-dose

其他结果措施

结果测量
措施说明
大体时间
Clinically relevant changes in blood pressure after supplementation
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in blood pressure (mmHg) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in aspartate aminotransferase
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in aspartate aminotransferase (U/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in red blood cell count
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in red blood cell count (x 10^12/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in heart rate after supplementation
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in heart rate (beats per minute) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in body temperature after supplementation
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in body temperature (°C) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in oxygen levels after supplementation
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in oxygen levels (%) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in alanine aminotransferase
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in alanine aminotransferase (U/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in alkaline phosphatase
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in alkaline phosphatase (U/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in total bilirubin
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in total bilirubin (micromole/litre) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in creatinine
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in creatinine (micromole/litre) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in sodium
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in sodium (mmol/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in potassium
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in potassium (mmol/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in chloride
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in chloride (mmol/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in estimated glomerular filtration rate
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in estimated glomerular filtration rate (mL/min/1.73 m^2) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in glucose
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in glucose (mmol/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in white blood cell count
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in white blood cell (x 10^9/L) count following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in platelet count
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in platelet count (x10^9/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in hemoglobin
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in hemoglobin (g/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in hematocrit
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in hematocrit (L/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in red blood cell indices (MCV)
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in MCV (fL) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in red blood cell indices (MCH)
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in MCH (pg) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in red blood cell indices (MCHC)
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in MCHC (g/L) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in RDW
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in RDW (%) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in red blood cell indices (MPV)
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
Clinically relevant changes in MPV (fL) following consumption of PG-containing beverages.
From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)

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。

合作者

调查人员

  • 首席研究员:David Crowley、KGK Science Inc.

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7月2日

初级完成 (估计的)

2026年8月1日

研究完成 (估计的)

2026年8月1日

研究注册日期

首次提交

2026年6月4日

首先提交符合 QC 标准的

2026年6月8日

首次发布 (实际的)

2026年6月12日

研究记录更新

最后更新发布 (实际的)

2026年7月8日

上次提交的符合 QC 标准的更新

2026年7月6日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

关键字

其他相关的 MeSH 术语

其他研究编号

  • 26ABAKC01

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 共享访问标准

Upon request (with justification provided), as agreed to by the sponsor. The confidentiality of the participants must be preserved and blinded.

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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