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

2026년 7월 6일 업데이트: 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

연구 개요

상태

모병

정황

개입 / 치료

연구 유형

중재적

등록 (추정된)

30

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

연구 장소

    • Ontario
      • London, Ontario, 캐나다, N5Y 5V6
        • 모병
        • KGK Science Inc.

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

  • 성인
  • 고령자

건강한 자원 봉사자를 받아들입니다

예

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 기초 과학
  • 할당: 해당 없음
  • 중재 모델: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
The maximum concentration of propylene glycol in serum
기간: 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.

2차 결과 측정

결과 측정
측정값 설명
기간
Serum PG Levels
기간: 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
기간: 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)
기간: 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-∞
기간: 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)
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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

기타 결과 측정

결과 측정
측정값 설명
기간
Clinically relevant changes in blood pressure after supplementation
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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
기간: 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)
기간: 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)
기간: 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)
기간: 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
기간: 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)
기간: 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)

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

스폰서

협력자

수사관

  • 수석 연구원: David Crowley, KGK Science Inc.

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (실제)

2026년 7월 2일

기본 완료 (추정된)

2026년 8월 1일

연구 완료 (추정된)

2026년 8월 1일

연구 등록 날짜

최초 제출

2026년 6월 4일

QC 기준을 충족하는 최초 제출

2026년 6월 8일

처음 게시됨 (실제)

2026년 6월 12일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 7월 8일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 7월 6일

마지막으로 확인됨

2026년 7월 1일

추가 정보

이 연구와 관련된 용어

기타 연구 ID 번호

  • 26ABAKC01

개별 참가자 데이터(IPD) 계획

개별 참가자 데이터(IPD)를 공유할 계획입니까?

예

IPD 공유 액세스 기준

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

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .