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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

2026年10月9日 更新者: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

研究概览

研究类型

介入性

注册 (估计的)

88

阶段

  • 不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习联系方式

学习地点

    • Ontario
      • London、Ontario、加拿大、N6B 3L1
        • KGK Science Inc.

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 45年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

描述

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

学习计划

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

研究是如何设计的?

设计细节

  • 主要用途:其他
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:四人间

武器和干预

参与者组/臂
干预/治疗
实验性的: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.

实验性的: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.

实验性的: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.

安慰剂比较: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.

研究衡量的是什么?

主要结果指标

结果测量
措施说明
大体时间
Percentage of grey hair between BioCopper1®, Restore Cu1, or Grow + Restore Cu1 and placebo, as assessed by HairMetrix
大体时间: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)

次要结果测量

结果测量
措施说明
大体时间
Change from baseline to Day 84 in percentage of grey hair between BioCopper1®, Restore Cu1, or Grow + Restore Cu1and placebo, as assessed by HairMetrix
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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

其他结果措施

结果测量
措施说明
大体时间
Incidence of post-emergent adverse events (AE)
大体时间: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
大体时间: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
大体时间: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)
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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
大体时间: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)

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2026年11月1日

初级完成 (估计的)

2027年7月1日

研究完成 (估计的)

2027年7月1日

研究注册日期

首次提交

2026年9月18日

首先提交符合 QC 标准的

2026年9月18日

首次发布 (实际的)

2026年9月24日

研究记录更新

最后更新发布 (实际的)

2026年10月15日

上次提交的符合 QC 标准的更新

2026年10月9日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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