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Two-Part Study of the Effects of the X39 Patch on Circulating GHK and GHK-Cu Levels in Healthy Adults

13. juli 2026 oppdatert av: LifeWave, Inc.

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.

Studieoversikt

Status

Har ikke rekruttert ennå

Studietype

Intervensjonell

Registrering (Antatt)

100

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

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

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

  • Voksen
  • Eldre voksen

Tar imot friske frivillige

Ja

Beskrivelse

Inclusion Criteria:

  1. Males and females 35 years and older
  2. 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
  3. Agrees to refrain from vigorous physical activity, alcohol consumption, and taking NSAIDs 24 hours prior to study visits
  4. Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study
  5. Willingness to complete questionnaires, diaries and to complete all clinic visits
  6. Provided voluntary, written, informed consent to participate in the study
  7. Healthy as determined by medical history 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 or sensitivity to the adhesive used for wearing the investigational patch
  3. Self-reported tattoos, skin conditions, or sensitive skin at or around the area of application
  4. Diagnosis with Wilson's disease
  5. 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)
  6. Unstable metabolic disease or chronic diseases as assessed by the QI
  7. Current or history of any significant diseases of the gastrointestinal tract as assessed by the QI
  8. Unstable hypertension. Treatment on a stable dose of medication for at least 3 months will be considered by the QI (See Section 7.3)
  9. Type I or Type II diabetes
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. Individuals with an autoimmune disease or are immune compromised as assessed by the QI
  16. Self-reported confirmation of a HIV-, Hepatitis B- and/or C-positive diagnosis as assessed by the QI
  17. Self-reported confirmation of blood/bleeding disorders as assessed by the QI
  18. Use of prescribed medical cannabinoid products
  19. Chronic use of cannabinoid products (>2 times/week). Occasional users will be required to washout and abstain for the duration of the study period
  20. 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
  21. Alcohol intake average of >2 standard drinks per day as assessed by the QI
  22. Alcohol or drug abuse within the last 12 months
  23. Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
  24. Individuals who are unable to give informed consent
  25. 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

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Firemannsrom

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Eksperimentell: 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.
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.
Placebo komparator: 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.
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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in GHK levels from baseline to Day 8
Tidsramme: Baseline (Day 0) to Day 8
Part 1. Change in GHK levels from baseline to Day 8
Baseline (Day 0) to Day 8
Change in GHK levels from baseline to Day 8 between the X39 patch and placebo
Tidsramme: Baseline (Day 0) to Day 8
Part 2. Change in GHK levels from baseline to Day 8 between the X39 patch and placebo
Baseline (Day 0) to Day 8
Change in GHK-Cu levels from baseline to Day 8
Tidsramme: Baseline (Day 0) to Day 8
Part 1. Change in GHK-Cu levels from baseline to Day 8
Baseline (Day 0) to Day 8
Change in GHK-Cu levels from baseline to Day 8 between the X39 patch and placebo
Tidsramme: Baseline (Day 0) to Day 8
Part 2. Change in GHK-Cu levels from baseline to Day 8 between the X39 patch and placebo
Baseline (Day 0) to Day 8

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Change in GHK levels from baseline to Day 2
Tidsramme: Baseline (Day 0) to Day 2
Part 1. Change in GHK levels from baseline to Day 2
Baseline (Day 0) to Day 2
Quality of Life, RAND SF-36
Tidsramme: Baseline (Day 0) to Day 8
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)
Baseline (Day 0) to Day 8
Change in GHK levels from baseline to Day 2 between the X39 patch and placebo
Tidsramme: Baseline (day 0) to Day 2
Part 2. Change in GHK levels from baseline to Day 2 between the X39 patch and placebo
Baseline (day 0) to Day 2
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
Tidsramme: Baseline (day 0) to Day 8
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.
Baseline (day 0) to Day 8
Change in GHK-Cu levels from baseline to Day 2
Tidsramme: Baseline (Day 0) to Day 2
Part 1. Change in GHK-Cu levels from baseline to Day 2
Baseline (Day 0) to Day 2
Change in GHK-Cu levels from baseline to Day 2 between the X39 patch and placebo
Tidsramme: Baseline (day 0) to Day 2
Part 2. Change in GHK-Cu levels from baseline to Day 2 between the X39 patch and placebo
Baseline (day 0) to Day 2

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Incidence of post-emergent adverse events (AE)
Tidsramme: Day 0 to Day 8
Incidence of post-emergent adverse events (AE)
Day 0 to Day 8
Clinically relevant changes in blood pressure after supplementation
Tidsramme: Day 0 to Day 8
Clinically relevant changes in blood pressure (mmHg) after supplementation
Day 0 to Day 8
Clinically relevant changes in sodium
Tidsramme: Day 0 to Day 8
Clinically relevant changes in sodium (mmol/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in heart rate after supplementation
Tidsramme: Day 0 to Day 8
Clinically relevant changes in heart rate (beats per minute) after supplementation
Day 0 to Day 8
Clinically relevant changes in potassium
Tidsramme: Day 0 to Day 8
Clinically relevant changes in potassium (mmol/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in chloride
Tidsramme: Day 0 to Day 8
Clinically relevant changes in chloride (mmol/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in estimated glomerular filtration rate
Tidsramme: Day 0 to Day 8
Clinically relevant changes in estimated glomerular filtration rate (mL/min/1.73 m^2) after supplementation
Day 0 to Day 8
Clinically relevant changes in glucose
Tidsramme: Day 0 to Day 8
Clinically relevant changes in glucose (mmol/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in creatinine
Tidsramme: Day 0 to Day 8
Clinically relevant changes in creatinine (micromole/litre) after supplementation
Day 0 to Day 8
Clinically relevant changes in aspartate aminotransferase
Tidsramme: Day 0 to Day 8
Clinically relevant changes in aspartate aminotransferase (U/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in alanine aminotransferase
Tidsramme: Day 0 to Day 8
Clinically relevant changes in alanine aminotransferase (U/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in alkaline phosphatase
Tidsramme: Day 0 to Day 8
Clinically relevant changes in alkaline phosphatase (U/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in bilirubin
Tidsramme: Day 0 to Day 8
Clinically relevant changes in bilirubin (micromole/litre) after supplementation
Day 0 to Day 8
Clinically relevant changes in red blood cell count
Tidsramme: Day 0 to Day 8
Clinically relevant changes in red blood cell count (x 10^12/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in white blood cell count
Tidsramme: Day 0 to Day 8
Clinically relevant changes in white blood cell count (x 10^9/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in platelet count
Tidsramme: Day 0 to Day 8
Clinically relevant changes in platelet count (x 10^9/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in hemoglobin
Tidsramme: Day 0 to Day 8
Clinically relevant changes in hemoglobin (g/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in hematocrit
Tidsramme: Day 0 to Day 8
Clinically relevant changes in hematocrit (L/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in red blood cell indices (MCV)
Tidsramme: Day 0 to Day 8
Clinically relevant changes in MCV (fL) after supplementation
Day 0 to Day 8
Clinically relevant changes in red blood cell indices (MCH)
Tidsramme: Day 0 to Day 8
Clinically relevant changes in MCH (pg) after supplementation
Day 0 to Day 8
Clinically relevant changes in red blood cell indices (MCHC)
Tidsramme: Day 0 to Day 8
Clinically relevant changes in MCHC (g/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in red blood cell indices (MPV)
Tidsramme: Day 0 to Day 8
Clinically relevant changes in MPV (fL) after supplementation
Day 0 to Day 8
Clinically relevant changes in RDW
Tidsramme: Day 0 to Day 8
Clinically relevant changes in RDW (%) after supplementation
Day 0 to Day 8

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Sponsor

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: David Crowley, KGK Science Inc.

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

1. januar 2027

Primær fullføring (Antatt)

1. april 2027

Studiet fullført (Antatt)

1. april 2027

Datoer for studieregistrering

Først innsendt

8. juli 2026

Først innsendt som oppfylte QC-kriteriene

13. juli 2026

Først lagt ut (Faktiske)

15. juli 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

15. juli 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

13. juli 2026

Sist bekreftet

1. juli 2026

Mer informasjon

Begreper knyttet til denne studien

Nøkkelord

Andre studie-ID-numre

  • 26LWCRL04

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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