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

2026年7月13日 更新者: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.

調査の概要

状態

まだ募集していません

研究の種類

介入

入学 (推定)

100

段階

  • 適用できない

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究場所

    • Ontario
      • London、Ontario、カナダ、N5Y 5V6
        • KGK Science Inc.

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

はい

説明

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

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:4倍

武器と介入

参加者グループ / アーム
介入・治療
実験的: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.
プラセボコンパレーター: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Change in GHK levels from baseline to Day 8
時間枠: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
時間枠: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
時間枠: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
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Change in GHK levels from baseline to Day 2
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

その他の成果指標

結果測定
メジャーの説明
時間枠
Incidence of post-emergent adverse events (AE)
時間枠: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
時間枠:Day 0 to Day 8
Clinically relevant changes in blood pressure (mmHg) after supplementation
Day 0 to Day 8
Clinically relevant changes in sodium
時間枠: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
時間枠: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
時間枠:Day 0 to Day 8
Clinically relevant changes in potassium (mmol/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in chloride
時間枠: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
時間枠: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
時間枠:Day 0 to Day 8
Clinically relevant changes in glucose (mmol/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in creatinine
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠:Day 0 to Day 8
Clinically relevant changes in hemoglobin (g/L) after supplementation
Day 0 to Day 8
Clinically relevant changes in hematocrit
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠:Day 0 to Day 8
Clinically relevant changes in MPV (fL) after supplementation
Day 0 to Day 8
Clinically relevant changes in RDW
時間枠:Day 0 to Day 8
Clinically relevant changes in RDW (%) after supplementation
Day 0 to Day 8

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

スポンサー

協力者

捜査官

  • 主任研究者:David Crowley、KGK Science Inc.

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (推定)

2027年1月1日

一次修了 (推定)

2027年4月1日

研究の完了 (推定)

2027年4月1日

試験登録日

最初に提出

2026年7月8日

QC基準を満たした最初の提出物

2026年7月13日

最初の投稿 (実際)

2026年7月15日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月15日

QC基準を満たした最後の更新が送信されました

2026年7月13日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

キーワード

その他の研究ID番号

  • 26LWCRL04

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米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

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