A Clinical Trial to Assess the Pharmacokinetic Profile of Propylene Glycol (PG) in Healthy Adults Following PG Exposure
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
注册 (估计的)
阶段
- 不适用
联系人和位置
学习联系方式
- 姓名:Erin Lewis, PhD
- 电话号码:248 1-226-242-4551
- 邮箱:elewis@kgkscience.com
学习地点
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Ontario
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London、Ontario、加拿大、N5Y 5V6
- 招聘中
- KGK Science Inc.
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参与标准
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
描述
Inclusion Criteria:
- Males and females 18 years and older
- Body Mass Index (BMI) between 18.5 to 29.9 kg/m2
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
- 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
- Willingness to complete diaries, food records, and to complete all clinic visits
- Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study
- Provided voluntary, written, informed consent to participate in the study
- Healthy as determined by medical history and laboratory results as assessed by the Qualified Investigator (QI)
Exclusion Criteria:
- Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
- Allergy, sensitivity, or intolerance, preventing consumption of investigational product ingredients and standardized meal
- Individuals with alcohol dehydrogenase deficiency as assessed by the QI
- Poor venous access as assessed by the QI
- 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
- 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.)
- 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
- Unstable metabolic disease or chronic diseases as assessed by the QI
- Current or history of any significant diseases of the gastrointestinal tract as assessed by the QI
- Unstable hypertension. Treatment on a stable dose of medication for at least 3 months will be considered by the QI (See Section 7.3)
- 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
- 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.)
- 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.
- Individuals with an autoimmune disease or are immune compromised as assessed by the QI.
- Self-reported confirmation of a HIV-, Hepatitis B- and/or C-positive diagnosis as assessed by the QI
- Self-reported confirmation of blood/bleeding disorders as assessed by the QI
- Use of prescribed cannabinoid products
- Chronic use of cannabinoid products (>2 times/week). Occasional users will be required to washout and abstain for the duration of the study period
- 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.
- Alcohol intake average of >1 standard drinks per day as assessed by the QI
- Alcohol or drug abuse within the last 12 months
- 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)
- Clinically significant abnormal laboratory results at screening as assessed by the QI
- Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
- Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
- Individuals who are unable to give informed consent
- 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
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 |
|---|---|
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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.
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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.
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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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The maximum concentration of propylene glycol in serum
大体时间:From pre-dose through 24 hours post-dose.
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The maximum concentration (Cmax) of propylene glycol (PG) in serum following consumption of one, two, or three PG-containing beverages.
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From pre-dose through 24 hours post-dose.
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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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Serum PG Levels
大体时间:Baseline (pre-dose) at each dosing visit
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The difference in baseline serum PG levels between each study period.
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Baseline (pre-dose) at each dosing visit
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Tmax
大体时间:From pre-dose through 24 hours post-dose
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Assessment of Tmax for PG following consumption of one, two, or three PG containing beverages.
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From pre-dose through 24 hours post-dose
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Area Under the Curve (AUC0-24hrs)
大体时间:From pre-dose through 24 hours post-dose
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Assessment of Area Under the Curve (AUC0-24hrs) for PG following consumption of one, two, or three PG containing beverages.
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From pre-dose through 24 hours post-dose
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AUC0-∞
大体时间:From pre-dose through 24 hours post-dose
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Assessment of AUC0-∞ for PG following consumption of one, two, or three PG containing beverages.
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From pre-dose through 24 hours post-dose
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Terminal elimination half-life (t1/2)
大体时间:From pre-dose through 24 hours post-dose
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Assessment of terminal elimination half-life (t1/2) for PG following consumption of one, two, or three PG containing beverages.
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From pre-dose through 24 hours post-dose
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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
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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.
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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
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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
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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.
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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
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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
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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.
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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
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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
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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.
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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
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其他结果措施
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
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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)
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Clinically relevant changes in blood pressure (mmHg) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in aspartate aminotransferase
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in aspartate aminotransferase (U/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in red blood cell count (x 10^12/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in heart rate (beats per minute) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in body temperature (°C) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in oxygen levels (%) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in alanine aminotransferase
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in alanine aminotransferase (U/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in alkaline phosphatase
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in alkaline phosphatase (U/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in total bilirubin
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in total bilirubin (micromole/litre) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in creatinine
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in creatinine (micromole/litre) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in sodium
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in sodium (mmol/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in potassium
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in potassium (mmol/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in chloride
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in chloride (mmol/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in estimated glomerular filtration rate (mL/min/1.73
m^2) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in glucose
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in glucose (mmol/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in white blood cell (x 10^9/L) count following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in platelet count
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in platelet count (x10^9/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in hemoglobin
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in hemoglobin (g/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in hematocrit
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in hematocrit (L/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in MCV (fL) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in MCH (pg) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in MCHC (g/L) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in RDW
大体时间:From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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Clinically relevant changes in RDW (%) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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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)
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Clinically relevant changes in MPV (fL) following consumption of PG-containing beverages.
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From screening (Day -45 to Day -1) through study completion (Visit 7, Day 12)
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合作者和调查者
研究记录日期
研究主要日期
学习开始 (实际的)
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
计划个人参与者数据 (IPD)
计划共享个人参与者数据 (IPD)?
IPD 共享访问标准
药物和器械信息、研究文件
研究美国 FDA 监管的药品
研究美国 FDA 监管的设备产品
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