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

6 de julho de 2026 atualizado por: 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

Visão geral do estudo

Status

Recrutamento

Intervenção / Tratamento

Tipo de estudo

Intervencional

Inscrição (Estimado)

30

Estágio

  • Não aplicável

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Locais de estudo

    • Ontario
      • London, Ontario, Canadá, N5Y 5V6
        • Recrutamento
        • KGK Science Inc.

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Sim

Descrição

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

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Ciência básica
  • Alocação: N / D
  • Modelo Intervencional: Atribuição sequencial
  • Mascaramento: Nenhum (rótulo aberto)

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Experimental: 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.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
The maximum concentration of propylene glycol in serum
Prazo: 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.

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Serum PG Levels
Prazo: 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
Prazo: 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)
Prazo: 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-∞
Prazo: 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)
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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

Outras medidas de resultado

Medida de resultado
Descrição da medida
Prazo
Clinically relevant changes in blood pressure after supplementation
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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
Prazo: 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)
Prazo: 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)
Prazo: 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)
Prazo: 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
Prazo: 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)
Prazo: 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)

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Colaboradores

Investigadores

  • Investigador principal: David Crowley, KGK Science Inc.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

2 de julho de 2026

Conclusão Primária (Estimado)

1 de agosto de 2026

Conclusão do estudo (Estimado)

1 de agosto de 2026

Datas de inscrição no estudo

Enviado pela primeira vez

4 de junho de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

8 de junho de 2026

Primeira postagem (Real)

12 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

8 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

6 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

Palavras-chave

Outros números de identificação do estudo

  • 26ABAKC01

Plano para dados de participantes individuais (IPD)

Planeja compartilhar dados de participantes individuais (IPD)?

SIM

Critérios de acesso de compartilhamento IPD

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

Informações sobre medicamentos e dispositivos, documentos de estudo

Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

Essas informações foram obtidas diretamente do site clinicaltrials.gov sem nenhuma alteração. Se você tiver alguma solicitação para alterar, remover ou atualizar os detalhes do seu estudo, entre em contato com register@clinicaltrials.gov. Assim que uma alteração for implementada em clinicaltrials.gov, ela também será atualizada automaticamente em nosso site .

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