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

6 juillet 2026 mis à jour par: 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

Aperçu de l'étude

Statut

Recrutement

Intervention / Traitement

Type d'étude

Interventionnel

Inscription (Estimé)

30

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Coordonnées de l'étude

Lieux d'étude

    • Ontario
      • London, Ontario, Canada, N5Y 5V6
        • Recrutement
        • KGK Science Inc.

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

  • Adulte
  • Adulte plus âgé

Accepte les volontaires sains

Oui

La description

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

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: Science basique
  • Répartition: N / A
  • Modèle interventionnel: Affectation séquentielle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: 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.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
The maximum concentration of propylene glycol in serum
Délai: 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.

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Serum PG Levels
Délai: 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
Délai: 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)
Délai: 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-∞
Délai: 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)
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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

Autres mesures de résultats

Mesure des résultats
Description de la mesure
Délai
Clinically relevant changes in blood pressure after supplementation
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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
Délai: 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)
Délai: 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)
Délai: 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)
Délai: 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
Délai: 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)
Délai: 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)

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Collaborateurs

Les enquêteurs

  • Chercheur principal: David Crowley, KGK Science Inc.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

2 juillet 2026

Achèvement primaire (Estimé)

1 août 2026

Achèvement de l'étude (Estimé)

1 août 2026

Dates d'inscription aux études

Première soumission

4 juin 2026

Première soumission répondant aux critères de contrôle qualité

8 juin 2026

Première publication (Réel)

12 juin 2026

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

8 juillet 2026

Dernière mise à jour soumise répondant aux critères de contrôle qualité

6 juillet 2026

Dernière vérification

1 juillet 2026

Plus d'information

Termes liés à cette étude

Mots clés

Autres numéros d'identification d'étude

  • 26ABAKC01

Plan pour les données individuelles des participants (IPD)

Prévoyez-vous de partager les données individuelles des participants (DPI) ?

OUI

Critères d'accès au partage IPD

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

Informations sur les médicaments et les dispositifs, documents d'étude

Étudie un produit pharmaceutique réglementé par la FDA américaine

Non

Étudie un produit d'appareil réglementé par la FDA américaine

Non

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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