At a glance
- What the study gets you
- Access to the study treatment being tested
- Type of study
- Interventional (receives a drug or procedure)
- Time in hospital
- In-person visits at study sites — visit count not specified by the sponsor
- Drug or intervention
- Mitopure Topical Formula (other)
- How long the study runs
- Study runs about 1 month (dates as stated)
- About the drug or intervention
- Mitopure Topical Formula — other: Topical skin serum containing Mitopure
- Patient visit burden
- Not specified by the sponsor
- Type of study
- Testing a treatment
- Ages
- 18 Years and over
- Who
- All
- Number of participants
- 40
- Started
- 2026-04-20
- Last checked
- 2026-06
Plain English Summary
What is this study?
- • Testing a new treatment for healthy adult
- • NA - 40 participants
- • The objective of this study is to investigate the safety of 1 topically applied test article containing Mitopure in a panel of healthy volunteers
Who can take part?
- • Ages 18 Years and over
- • Diagnosed with healthy adult
Where?
- • Manchester - PCR Corp
This is a simplified summary. Always discuss with your doctor before making any decisions.
About This Trial
The objective of this study is to investigate the safety of 1 topically applied test article containing Mitopure in a panel of healthy volunteers.
Healthy Adult
How this trial compares with your answers
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What we know so far
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Preliminary match based on your answers. Full eligibility requires on-site assessment including medical history, physical exam, and lab tests. This does not guarantee enrolment.
Eligibility at a Glance
Key info
- Age: 18 Years and over
- Who can join: All genders
What the study is looking for
- ✓Healthy male and female participants aged 18+.
- ✓Participant has signed a written agreement to take part.
- ✓Participant must agree to refrain from taking any new medications or herbal supplements during the study, unless...
- ✓Participant does not have grade of 3 or higher of any skin attribute per the grading scale.
- ✓Participant is willing to ONLY use the test article on themselves during the study as instructed and not use other...
Who cannot take part
- ✗Participant is pregnant, nursing, or planning to become pregnant (by verbal response only).
- ✗Participant has a current skin disease of any type (e.g., eczema, psoriasis, rosacea, atopic dermatitis, vitiligo).
- ✗Participant has a known allergy to face serum products, or the ingredients included in the test article.
- ✗Participant has a history of malignant disease.
- ✗Participant has cuts, scratches, abrasions, rashes, scarring, birthmarks, or tattoos on their face that may...
See the full criteria
Inclusion Criteria:
* Healthy male and female participants aged 18+.
* Participant has signed a written Informed Consent.
* Participant must agree to refrain from taking any new medications or herbal supplements during the study, unless permitted by the investigator.
* Participant does not have grade of 3 or higher of any skin attribute per the grading scale.
* Participant is willing to ONLY use the test article on themselves during the study as instructed and not use other facial serum products.
* Participant is willing to attend all study visits and to follow the study instructions and prohibitions.
* Participant must agree to refrain from using any new facial serum products, cleansers, laundry detergents, fragrances while participating in this study.
Exclusion Criteria:
* Participant is pregnant, nursing, or planning to become pregnant (by verbal response only).
* Participant has a current skin disease of any type (e.g., eczema, psoriasis, rosacea, atopic dermatitis, vitiligo).
* Participant has a known allergy to face serum products, or the ingredients included in the test article.
* Participant has a history of malignant disease.
* Participant has cuts, scratches, abrasions, rashes, scarring, birthmarks, or tattoos on their face that may interfere with assessments.
* Participant has a significant past medical history of hepatic, renal, cardiac, pulmonary, digestive, haematological, neurological, locomotor or psychiatric disease.
* Participant has a known sensitivity to the test article, similar materials, or their constituents.
* Treatment or medication containing sympathomimetics, antihistamines or corticosteroids in the seven days prior to study start.
* Medical condition that may affect study data or participant safety which in the opinion of the Investigator would compromise the safety of the participant or study results.
* History of poor cooperation, non-compliance, or unreliability.
* Investigator deems the participant an unsuitable candidate for the study.
Where Is This Study? (1 UK site)
PCR Corp
Manchester M13 0AF, United Kingdom
Data sourced from ClinicalTrials.gov · Last verified: 2026-06