- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07706361
Two-Part Study of the Effects of the X39 Patch on Circulating GHK and GHK-Cu Levels in Healthy Adults
A Two-part Study Investigating the Effect of the X39 Patch on Circulating Blood Levels of GHK and GHK-Cu in a Healthy Adult Population
The goal of this clinical trial is to investigate GHK and GHK-Cu blood levels pre- and post-intervention in healthy adults, and to investigate the efficacy of X39 patch on GHK and GHK-Cu blood levels in healthy adults compared to a placebo. The main questions it aims to answer are:
- What is the change in GHK and GHK-Cu levels from baseline to Day 8?
- What is the difference in the change in GHK and GHK-Cu levels from baseline to Day 8 between the X39 patch and placebo? Researchers will compare X39 patches to placebo patches to evaluate their effects on circulating blood levels of GHK and GHK-Cu in healthy adults.
Participants will be asked to complete a questionnaire and use the X39 patch or placebo patch.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Type d'étude
Inscription (Estimé)
Phase
- N'est pas applicable
Contacts et emplacements
Coordonnées de l'étude
- Nom: Erin Lewis, PhD
- Numéro de téléphone: +248 1-226-242-4551
- E-mail: elewis@kgkscience.com
Lieux d'étude
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Ontario
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London, Ontario, Canada, N5Y 5V6
- KGK Science Inc.
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
- Males and females 35 years and older
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, alcohol consumption, and taking NSAIDs 24 hours prior to study visits
- Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study
- Willingness to complete questionnaires, diaries and to complete all clinic visits
- Provided voluntary, written, informed consent to participate in the study
- Healthy as determined by medical history as assessed by the Qualified Investigator (QI)
Exclusion Criteria:
- Individuals who are pregnant, breast feeding, or planning to become pregnant during the study
- Allergy or sensitivity to the adhesive used for wearing the investigational patch
- Self-reported tattoos, skin conditions, or sensitive skin at or around the area of application
- Diagnosis with Wilson's disease
- Current use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the efficacy of the investigational product (Sections 7.3.1 and 7.3.2)
- 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)
- Type I or Type II diabetes
- 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
- 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
- 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 medical 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 tobacco or nicotine products in the past six months, as assessed by the QI. Occasional users will be required to washout and abstain for the duration of the study period
- Alcohol intake average of >2 standard drinks per day as assessed by the QI
- Alcohol or drug abuse within the last 12 months
- 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
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Quadruple
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
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Expérimental: X39 Patch
Beginning on Day 1, participants will apply the patch daily until Day 7 or the day prior to their last study visit (Visit 3).
Participants will apply the patch to the back of the neck (acupuncture point GV14) or directly below the belly button (acupuncture point CV6) on clean, dry skin first thing each morning and remove after approximately 12 hours later or before bed.
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Beginning on Day 1, participants will apply the patch daily until Day 7 or the day prior to their last study visit (Visit 3).
Participants will apply the patch to the back of the neck (acupuncture point GV14) or directly below the belly button (acupuncture point CV6) on clean, dry skin first thing each morning and remove after approximately 12 hours later or before bed.
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Comparateur placebo: Placebo patch
Beginning on Day 1, participants will apply the patch daily until Day 7 or the day prior to their last study visit (Visit 3).
Participants will apply the patch to the back of the neck (acupuncture point GV14) or directly below the belly button (acupuncture point CV6) on clean, dry skin first thing each morning and remove after approximately 12 hours later or before bed.
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Beginning on Day 1, participants will apply the patch daily until Day 7 or the day prior to their last study visit (Visit 3).
Participants will apply the patch to the back of the neck (acupuncture point GV14) or directly below the belly button (acupuncture point CV6) on clean, dry skin first thing each morning and remove after approximately 12 hours later or before bed.
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Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in GHK levels from baseline to Day 8
Délai: Baseline (Day 0) to Day 8
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Part 1. Change in GHK levels from baseline to Day 8
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Baseline (Day 0) to Day 8
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Change in GHK levels from baseline to Day 8 between the X39 patch and placebo
Délai: Baseline (Day 0) to Day 8
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Part 2. Change in GHK levels from baseline to Day 8 between the X39 patch and placebo
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Baseline (Day 0) to Day 8
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Change in GHK-Cu levels from baseline to Day 8
Délai: Baseline (Day 0) to Day 8
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Part 1. Change in GHK-Cu levels from baseline to Day 8
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Baseline (Day 0) to Day 8
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Change in GHK-Cu levels from baseline to Day 8 between the X39 patch and placebo
Délai: Baseline (Day 0) to Day 8
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Part 2. Change in GHK-Cu levels from baseline to Day 8 between the X39 patch and placebo
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Baseline (Day 0) to Day 8
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Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Change in GHK levels from baseline to Day 2
Délai: Baseline (Day 0) to Day 2
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Part 1. Change in GHK levels from baseline to Day 2
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Baseline (Day 0) to Day 2
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Quality of Life, RAND SF-36
Délai: Baseline (Day 0) to Day 8
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Part 1. Change in quality of life from baseline to Days 2 and 8, as assessed by the RAND 36-item Short-Form Health Survey (RAND SF-36)
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Baseline (Day 0) to Day 8
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Change in GHK levels from baseline to Day 2 between the X39 patch and placebo
Délai: Baseline (day 0) to Day 2
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Part 2. Change in GHK levels from baseline to Day 2 between the X39 patch and placebo
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Baseline (day 0) to Day 2
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Change in Quality of Life from Baseline to Days 2 and 8 (RAND 36-Item Short Form Health Survey - RAND SF-36) Between X39 Patch and Placebo
Délai: Baseline (day 0) to Day 8
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Part 2. Change in quality of life from baseline to Days 2 and 8, as assessed by the RAND 36-Item Short Form Health Survey (RAND SF-36), between the X39 patch and placebo.
This questionnaire measures nine scales including physical functioning, role limitations due to physical health, role limitations due to emotional health, pain, general health, energy/fatigue, social functioning, emotional well-being, and health transition.
The scores range from 0 to 100 where higher scores indicate a better state of health.
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Baseline (day 0) to Day 8
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Change in GHK-Cu levels from baseline to Day 2
Délai: Baseline (Day 0) to Day 2
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Part 1. Change in GHK-Cu levels from baseline to Day 2
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Baseline (Day 0) to Day 2
|
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Change in GHK-Cu levels from baseline to Day 2 between the X39 patch and placebo
Délai: Baseline (day 0) to Day 2
|
Part 2. Change in GHK-Cu levels from baseline to Day 2 between the X39 patch and placebo
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Baseline (day 0) to Day 2
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Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
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Incidence of post-emergent adverse events (AE)
Délai: Day 0 to Day 8
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Incidence of post-emergent adverse events (AE)
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Day 0 to Day 8
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Clinically relevant changes in blood pressure after supplementation
Délai: Day 0 to Day 8
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Clinically relevant changes in blood pressure (mmHg) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in sodium
Délai: Day 0 to Day 8
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Clinically relevant changes in sodium (mmol/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in heart rate after supplementation
Délai: Day 0 to Day 8
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Clinically relevant changes in heart rate (beats per minute) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in potassium
Délai: Day 0 to Day 8
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Clinically relevant changes in potassium (mmol/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in chloride
Délai: Day 0 to Day 8
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Clinically relevant changes in chloride (mmol/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in estimated glomerular filtration rate
Délai: Day 0 to Day 8
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Clinically relevant changes in estimated glomerular filtration rate (mL/min/1.73
m^2) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in glucose
Délai: Day 0 to Day 8
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Clinically relevant changes in glucose (mmol/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in creatinine
Délai: Day 0 to Day 8
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Clinically relevant changes in creatinine (micromole/litre) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in aspartate aminotransferase
Délai: Day 0 to Day 8
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Clinically relevant changes in aspartate aminotransferase (U/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in alanine aminotransferase
Délai: Day 0 to Day 8
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Clinically relevant changes in alanine aminotransferase (U/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in alkaline phosphatase
Délai: Day 0 to Day 8
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Clinically relevant changes in alkaline phosphatase (U/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in bilirubin
Délai: Day 0 to Day 8
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Clinically relevant changes in bilirubin (micromole/litre) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in red blood cell count
Délai: Day 0 to Day 8
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Clinically relevant changes in red blood cell count (x 10^12/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in white blood cell count
Délai: Day 0 to Day 8
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Clinically relevant changes in white blood cell count (x 10^9/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in platelet count
Délai: Day 0 to Day 8
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Clinically relevant changes in platelet count (x 10^9/L) after supplementation
|
Day 0 to Day 8
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Clinically relevant changes in hemoglobin
Délai: Day 0 to Day 8
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Clinically relevant changes in hemoglobin (g/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in hematocrit
Délai: Day 0 to Day 8
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Clinically relevant changes in hematocrit (L/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in red blood cell indices (MCV)
Délai: Day 0 to Day 8
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Clinically relevant changes in MCV (fL) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in red blood cell indices (MCH)
Délai: Day 0 to Day 8
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Clinically relevant changes in MCH (pg) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in red blood cell indices (MCHC)
Délai: Day 0 to Day 8
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Clinically relevant changes in MCHC (g/L) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in red blood cell indices (MPV)
Délai: Day 0 to Day 8
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Clinically relevant changes in MPV (fL) after supplementation
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Day 0 to Day 8
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Clinically relevant changes in RDW
Délai: Day 0 to Day 8
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Clinically relevant changes in RDW (%) after supplementation
|
Day 0 to Day 8
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Collaborateurs et enquêteurs
Parrainer
Collaborateurs
Les enquêteurs
- Chercheur principal: David Crowley, KGK Science Inc.
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
Étudie un produit d'appareil réglementé par la FDA américaine
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