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A Clinical Trial to Investigate the Efficacy of BioCopper1®, Restore Cu1, and Grow + Restore Cu1 on Hair and Skin Improvements in Healthy Adults

9. Oktober 2026 aktualisiert von: Mitosynergy LLC

A Triple-blind, Randomized, Placebo-controlled, Parallel Clinical Trial to Investigate the Efficacy of BioCopper1®, Restore Cu1, and Grow + Restore Cu1 on Hair and Skin Improvements in Healthy Adults

The goal of this clinical trial is to investigate the efficacy of BioCopper1®, Restore Cu1, and Grow + Restore Cu1 on grey hair, hair growth, and/or skin improvements in healthy adults. The main question it aims to answer is: what is the change from baseline to Day 168 in percentage of grey hair between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by HairMetrix? Researchers will compare the investigational products to a placebo to determine their effectiveness. Participants will be asked to:

  • Have their blood pressure, heart rate, height, and weight measurements taken
  • Have their blood samples collected
  • Complete questionnaires and a study diary
  • Be assessed using the VISIA imaging system, Corneometer, and Cutometer
  • Consume BioCopper1®, Restore Cu1, Grow + Restore Cu1, or placebo

Studienübersicht

Studientyp

Interventionell

Einschreibung (Geschätzt)

88

Phase

  • Unzutreffend

Kontakte und Standorte

Dieser Abschnitt enthält die Kontaktdaten derjenigen, die die Studie durchführen, und Informationen darüber, wo diese Studie durchgeführt wird.

Studienkontakt

Studienorte

    • Ontario
      • London, Ontario, Kanada, N6B 3L1
        • KGK Science Inc.

Teilnahmekriterien

Forscher suchen nach Personen, die einer bestimmten Beschreibung entsprechen, die als Auswahlkriterien bezeichnet werden. Einige Beispiele für diese Kriterien sind der allgemeine Gesundheitszustand einer Person oder frühere Behandlungen.

Zulassungskriterien

Studienberechtigtes Alter

18 Jahre bis 45 Jahre (Erwachsene)

Akzeptiert gesunde Freiwillige

Ja

Studienberechtigte Geschlechter

Alle

Beschreibung

Inclusion Criteria:

  1. Males and females aged 18 to 45 years, inclusive

  2. Stable body weight defined as a <5% change in body weight in the three months prior to baseline as assessed by the Qualified Investigator (QI)

  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 A 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. Visual confirmation of ≥ 5% and ≤ 20% of grey hair at screening

  5. Pattern hair loss (Savin/Ludwig Scale Criteria I-2 (early-moderate hair loss) to II-2 (moderate hair loss) for females and Hamilton-Norwood Scale Criteria II to IV-A for males) at screening as assessed by the QI (onset of hair loss/thinning not to correspond with hormonal birth control or other recent onset of new medications, as assessed by the QI)

  6. Agrees to maintain normal hair cleaning (frequency and use of non-medicated shampoo and/or conditioner) and general hair regime for the study period (including use of heated hair tools)

  7. Agrees to maintain hairstyle for the study period

  8. Agrees to avoid colouring hair 6 weeks prior to screening/baseline and each clinic visit

  9. Agrees to maintain normal skin care routine for the study period and avoid use of cosmetic products (e.g, cleansing products, creams, makeup) on the day of clinic visits

  10. Agrees to avoid excessive sun exposure and engage in safe sun practices for the duration of the study period

  11. Agrees to maintain current lifestyle habits (diet, physical activity, medications, supplements, and sleep) as much as possible throughout the study

  12. Provided voluntary, written, informed consent to participate in the study

  13. Healthy as determined by medical history and laboratory results as assessed by the 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, comparator, or placebo ingredients
  3. Infections or dermatological conditions of the scalp and/or face
  4. Significant life or traumatic event that may be associated with acute hair loss (e.g., postpartum, job loss, death of a family member), as assessed by a QI
  5. Current diagnosis or history of Lyme disease
  6. History of or current diseases (e.g., alopecia areata) or conditions (e.g., trichotillomania, telogen effluvium, polycystic ovary syndrome) contributing to hair loss or thinning
  7. Use of hair treatments, medications, or therapies for the purpose of regrowing and/or thickening (e.g., scalp treatments, hair transplantation surgery), as assessed by the QI
  8. Individuals with hair extensions or planning on getting hair extensions during the study period, as assessed by the QI
  9. Individuals with known disorders of copper metabolism (e.g., Wilson disease)
  10. 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
  11. Unstable metabolic disease or chronic diseases as assessed by the QI
  12. Current or history of any significant diseases of the gastrointestinal tract as assessed by the QI
  13. Unstable hypertension. Treatment on a stable dose of medication for at least 3 months will be considered by the QI (See Section 7.3)
  14. Type I or Type II diabetes
  15. 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
  16. 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
  17. Current diagnosis with biliary disorders
  18. 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
  19. 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
  20. Individuals with an autoimmune disease or are immune compromised as assessed by the QI
  21. Self-reported confirmation of a Human Immunodeficiency Virus (HIV)-, Hepatitis B- and/or C-positive diagnosis as assessed by the QI
  22. Self-reported confirmation of blood/bleeding disorders as assessed by the QI
  23. Use of prescribed cannabinoid products as assessed by the QI
  24. Chronic use of cannabinoid products (>2 times/week). Occasional users will be required to washout and abstain for the duration of the study period
  25. 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
  26. Alcohol intake average of >2 standard drinks per day as assessed by the QI
  27. Alcohol or drug abuse within the last 12 months
  28. Current use of prescribed and/or over-the-counter (OTC) medications, supplements, and/or consumption of food/drinks that may impact the efficacy and/or safety of the investigational product (Section 7.3)
  29. Clinically significant abnormal laboratory results at screening as assessed by the QI
  30. Blood donation 30 days prior to baseline, during the study, or a planned donation within 30 days of the last study visit
  31. Participation in other clinical research studies 30 days prior to baseline, as assessed by the QI
  32. Individuals who are unable to give informed consent
  33. 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

Studienplan

Dieser Abschnitt enthält Einzelheiten zum Studienplan, einschließlich des Studiendesigns und der Messung der Studieninhalte.

Wie ist die Studie aufgebaut?

Designdetails

  • Hauptzweck: Sonstiges
  • Zuteilung: Zufällig
  • Interventionsmodell: Parallele Zuordnung
  • Maskierung: Vervierfachen

Waffen und Interventionen

Teilnehmergruppe / Arm
Intervention / Behandlung
Experimental: BioCopper1

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Experimental: Restore Cu1

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Experimental: Grow + Restore Cu1

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Placebo-Komparator: Placebo

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Starting the day following their baseline B visit (Day 1), participants will be instructed to take one dose (one capsule) with water twice daily with food until the day prior to their end of study visit (Day 167). Participants will be instructed to not take any zinc or N-acetylcysteine supplements within 4 hours of dose.

Was misst die Studie?

Primäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Percentage of grey hair between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by HairMetrix
Zeitfenster: Visit 1 (day -3) to visit 5 (day 168)

Change from baseline to Day 168 in percentage of grey hair between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by HairMetrix.

Visit 1 (day -3) to visit 5 (day 168)

Sekundäre Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Change from baseline to Day 84 in percentage of grey hair between BioCopper1®, Restore Cu1, or Grow + Restore Cu1and placebo, as assessed by HairMetrix
Zeitfenster: Visit 1 (day -3) to visit 3 (day 84)

Change from baseline to Day 84 in percentage of grey hair between BioCopper1®, Restore Cu1, or Grow + Restore Cu1and placebo, as assessed by HairMetrix

Visit 1 (day -3) to visit 3 (day 84)
Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by ratio of vellus to terminal hairs
Zeitfenster: Visit 1 (day -3) to day 87

Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by ratio of vellus to terminal hairs

Visit 1 (day -3) to day 87
Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by hair density
Zeitfenster: Visit 1 (day -3) to day 87

Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by hair density

Visit 1 (day -3) to day 87
Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by hair fiber diameter
Zeitfenster: Visit 1 (day -3) to day 87

Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by hair fiber diameter

Visit 1 (day -3) to day 87
Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by percentage of hairs in the anagen phase
Zeitfenster: Visit 1 (day -3) to day 87

Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by percentage of hairs in the anagen phase

Visit 1 (day -3) to day 87
Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by percentage of hairs in the telogen phase
Zeitfenster: Visit 1 (day -3) to day 87

Change from baseline to Day 87 in hair growth and density between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by percentage of hairs in the telogen phase

Visit 1 (day -3) to day 87
Change from baseline to Day 84 between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo as assessed by Corneometer and Cutometer
Zeitfenster: Visit 1 (day -3) to day 84

Change from baseline to Day 84 between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo as assessed by Corneometer and Cutometer. The devices measure skin elasticity, firmness and hydration.

Visit 1 (day -3) to day 84
Change from baseline to Day 84 between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo as assessed by VISIA
Zeitfenster: Visit 1 (day -3) to day 84

Change from baseline to Day 84 between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo as assessed by VISIA. The device measures wrinkles, texture, and age spots.

Visit 1 (day -3) to day 84
Difference in perceived skin and hair improvements at Day 84 and Day 168 between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo
Zeitfenster: Day 84 and Day 168

Difference in perceived skin and hair improvements at Day 84 and Day 168 between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by the Global Aesthetic Improvement Scales (GAISs)

Day 84 and Day 168
Change from baseline to Day 84 and Day 168 in energy/fatigue and sleep between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo
Zeitfenster: Visit 1 (day -3) to day 84 and day 168

Change from baseline to Day 84 and Day 168 in energy/fatigue and sleep between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by energy and sleep Likert scales

Visit 1 (day -3) to day 84 and day 168

Andere Ergebnismessungen

Ergebnis Maßnahme
Maßnahmenbeschreibung
Zeitfenster
Incidence of post-emergent adverse events (AE)
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Incidence of post-emergent adverse events (AE)

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in blood pressure
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in blood pressure (mm HG) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in heart rate
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in heart rate (bpm) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Gastrointestinal symptoms, as assessed by the Modified Gastrointestinal Symptom Rating Scale (GSRS)
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Gastrointestinal symptoms, as assessed by the Modified Gastrointestinal Symptom Rating Scale (GSRS). The modified GSRS has been revised to improve participant understanding and includes 15 questions with a four-point Likert scale from 0-3. The total score ranges from 0 to 45, with lower scores indicating better gastrointestinal symptoms and higher scores indicating worse gastrointestinal symptoms.

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in aspartate aminotransferase
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in aspartate aminotransferase (U/L) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in alanine aminotransferase
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in alanine aminotransferase (U/L) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in alkaline phosphatase
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in alkaline phosphatase (U/L) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in total bilirubin
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in total bilirubin (micromole/litre) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in creatinine
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in creatinine (micromole/litre) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in sodium
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in sodium (mmol/L) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in potassium
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in potassium (mmol/L) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in chloride
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in chloride (mmol/L) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in estimated glomerular filtration rate
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in estimated glomerular filtration rate (mL/min/1.73 m^2) after supplementation

Visit 1 (day -3) to Visit 5 (day 168)
Clinically relevant changes in complete blood count
Zeitfenster: Visit 1 (day -3) to Visit 5 (day 168)

Clinically relevant changes in complete blood count after supplementation

Visit 1 (day -3) to Visit 5 (day 168)

Mitarbeiter und Ermittler

Hier finden Sie Personen und Organisationen, die an dieser Studie beteiligt sind.

Sponsor

Mitarbeiter

Studienaufzeichnungsdaten

Diese Daten verfolgen den Fortschritt der Übermittlung von Studienaufzeichnungen und zusammenfassenden Ergebnissen an ClinicalTrials.gov. Studienaufzeichnungen und gemeldete Ergebnisse werden von der National Library of Medicine (NLM) überprüft, um sicherzustellen, dass sie bestimmten Qualitätskontrollstandards entsprechen, bevor sie auf der öffentlichen Website veröffentlicht werden.

Haupttermine studieren

Studienbeginn (Geschätzt)

1. November 2026

Primärer Abschluss (Geschätzt)

1. Juli 2027

Studienabschluss (Geschätzt)

1. Juli 2027

Studienanmeldedaten

Zuerst eingereicht

18. September 2026

Zuerst eingereicht, das die QC-Kriterien erfüllt hat

18. September 2026

Zuerst gepostet (Tatsächlich)

24. September 2026

Studienaufzeichnungsaktualisierungen

Letztes Update gepostet (Tatsächlich)

15. Oktober 2026

Letztes eingereichtes Update, das die QC-Kriterien erfüllt

9. Oktober 2026

Zuletzt verifiziert

1. Oktober 2026

Mehr Informationen

Begriffe im Zusammenhang mit dieser Studie

Andere Studien-ID-Nummern

  • 26MSKGC01

Arzneimittel- und Geräteinformationen, Studienunterlagen

Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt

Nein

Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt

Nein

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