The Effect of Urolithin A (Mitopure®) Supplementation on Muscle Strength in Healthy Middle-Aged Adults

NCT ID: NCT07231783

Last Updated: 2025-12-12

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: NA
• Total Enrollment: 120 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2025-12-10
• Study Completion Date: 2027-10-31

Brief Summary

This is a randomised, double-blind, placebo-controlled, parallel study to assess the effects of Urolithin A (Mitopure®) supplementation on muscle strength and performance in healthy middle-aged adults. Participants will be randomized to consume Mitopure® (500 mg), Mitopure® (1000 mg), or placebo once daily for 6 months.

Conditions

Healthy Aging; Muscle Function

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: BASIC_SCIENCE
• Blinding Strategy: TRIPLE

Study Groups

Placebo

Group Type: PLACEBO_COMPARATOR

Placebo

Intervention Type: DIETARY_SUPPLEMENT

Placebo softgels

500 mg Mitopure®

Group Type: EXPERIMENTAL

Mitopure® 500mg

Intervention Type: DIETARY_SUPPLEMENT

Softgels providing 500 mg of Mitopure®

1000 mg Mitopure®

Group Type: EXPERIMENTAL

Mitopure® 1000mg

Intervention Type: DIETARY_SUPPLEMENT

Softgels providing 1000 mg of Mitopure®

Interventions

Placebo

Placebo softgels

Intervention Type: DIETARY_SUPPLEMENT

Mitopure® 500mg

Softgels providing 500 mg of Mitopure®

Intervention Type: DIETARY_SUPPLEMENT

Mitopure® 1000mg

Softgels providing 1000 mg of Mitopure®

Intervention Type: DIETARY_SUPPLEMENT

Eligibility Criteria

Inclusion Criteria

• 1. Be able to give written informed consent.
• 2. Be between 40 to 65 years of age, inclusive.
• 3. Has a BMI between 25.0 and 34.9 kg/m2.
• 4. Low physical activity levels as assessed by the International Physical Activity Questionnaire (IPAQ).
• 5. Participants with low VO2 peak (defined as <35 mL/kg/min via the ergometer prior to baseline).
• 6. Willing to avoid exercising 48-h prior to study visits and maintain low physical activity status for the duration of the study.
• 7. Willing to avoid caffeine and other stimulants (e.g., energy drinks) 12-h before exercise as per study guidelines.
• 8. Willing to consume the Study Product daily for the duration of the study.

Exclusion Criteria

• 1. Participants who are pregnant or wish to become pregnant during the study or who are lactating and/or currently breastfeeding.
• 2. Participants currently of biological childbearing potential, but not using a continuous effective method of contraception, as outlined below:

• a. Complete abstinence from intercourse two weeks prior to administration of the Study Product, throughout the clinical study, until the completion of follow-up procedures or for two weeks following discontinuation of the Study Product in cases where Participant discontinues the study prematurely. (Participants utilising this method must agree to use an alternate method of contraception if they should become sexually active and will be queried on whether they have been abstinent in the preceding two weeks when they present to the clinic for the final visit).
• b. Has a male sexual partner who is surgically sterilised prior to the Screening Visit and is the only male sexual partner for that Participant.
• c. Sexual partner(s) is/are exclusively female.
• d. Use of acceptable method of contraception, such as a spermicide, mechanical barrier (e.g., male condom, female diaphragm), tubal ligation, or contraceptive pill. The Participant must be using this method for at least one week prior to and one week following the end of the study.
• e. Use of any intrauterine device (IUD) or contraceptive implant. The Participant must have the device inserted at least two weeks prior to the first screening visit, throughout the study, and two weeks following the end of the study.
• 3. Participants with history of drug and/or alcohol abuse at the time of enrolment. (Drinks more than nationally recommended units per week (>11 units for women; >17 units for men); alcohol/substance abuse disorder).
• 4. Participants consuming large quantities of pomegranate juice or walnuts or frequent consumers of raspberries, strawberries or cloudberries (2-week washout).
• 5. Chronic nicotine use.
• 6. Participants who are unable to swallow capsules.
• 7. Is hypersensitive to or has dietary restrictions for any of the components of the Study Product e.g., gelatine
• 8. Unstable body weight or recent participation in a weight loss program (within 12-weeks prior to screening).
• 9. Has any significant acute or chronic coexisting health conditions that would prevent them from fulfilling the study requirements, put the Participant at risk or would confound the interpretation of the study results as judged by the investigator on the basis of medical history and routine laboratory test results. Excluded health conditions include:

• a. Major illness/surgery in the 12-weeks prior to screening
• b. Diagnosed cardiovascular disease (NHYA Class III or IV congestive heart failure, atrial fibrillation, uncontrolled arrhythmia, uncontrolled hypertension)
• c. Diagnosed liver disease (cirrhosis, end stage liver disease)
• d. Diagnosed kidney disease (stage 3b or 4 chronic kidney disease, or kidney failure)
• e. Diagnosed gastrointestinal disease (IBS/IBD, diarrhoea, Acid Reflux)
• f. Uncontrolled thyroid conditions
• g. Uncontrolled diabetes
• h. Metallic implants
• i. Conditions requiring chemotherapy or immunotherapy.
• 10. Current or recent use of a medication that the investigator believes would interfere with the objectives of the study or pose a safety risk or confound the interpretation of the study results. Prohibited medications include:

• a. Statins or other medications known to impair mitochondrial function.
• b. Anxiolytics, antidepressants, sedative hypnotics (in the 8 weeks prior to visit 1)
• c. Antipsychotics, monoamine Oxidase Inhibitors (in the 8 weeks prior to visit 1)
• d. Oral anti- infective (antibiotics, antivirals, antifungals) for acute infections (in the 12-weeks prior to visit 1)
• e. Proton pump inhibitors (PPIs) (in the 4 weeks prior to visit 1)
• f. Corticosteroids (> 5mg per day in the past 4 weeks prior to visit 1)
• g. GLP-1 agonists (in the 8 weeks prior to visit 1)
• 11. Current or recent (in the past 6-weeks prior to Visit 1) use of prohibited nutritional or non-nutritional supplements that the investigator believes would interfere with the objectives of the study or pose a safety risk or confound the interpretation of the study results. Prohibited supplements include:

• a. Mitopure® containing supplements
• b. Supplements for muscle strengthening/building or mitochondrial boosting supplements (e.g. high protein, Vitamin B3 [and precursors], L-carnitine, CoQ10, NAD+, resveratrol)
• 12. Blood donation in the 8-weeks prior to screening.
• 13. Individuals who, in the opinion of the investigator, are considered to be poor attendees or unlikely for any reason to be able to comply with the study.
• 14. Participants may not be participating in other clinical studies. If the participant has previously taken part in an experimental study (physical or muscle performance), the Investigator must ensure sufficient time has elapsed before entry to this study to ensure the integrity of the results.

• Minimum Eligible Age: 40 Years
• Maximum Eligible Age: 65 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Atlantia Food Clinical Trials

INDUSTRY

Sponsor Role: collaborator

Amazentis SA

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Atlantia Clinical Trials

Cork, , Ireland

Site Status: RECRUITING

Countries

Ireland

Central Contacts

Brad Currier, PhD

Role: CONTACT

bcurrier@timeline.com

+41 215521272

Anurag Singh, MD, PhD

Role: CONTACT

Facility Contacts

Timothy Dinan, MD

Role: primary

tdinan@atlantiatrials.com

+353 (0) 21-430-7442

Other Identifiers

AFCRO-197

Identifier Type: -

Identifier Source: org_study_id