A Clinical Trial to Assess the Pharmacokinetic Profile of Three Coenzyme Q10 Formulations in Healthy Adults
NCT07255079 · Status: NOT_YET_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 20
Last updated 2025-11-28
Summary
The goal of this clinical trial is to assess the pharmacokinetic profile of three Coenzyme Q10 formulations in healthy adults. The main question it aims to answer is:
What is the difference in the bioavailability of three Coenzyme Q10 (CoQ10) formulations as assessed by the incremental area-under-the-curve (AUC) from time 0 to the last measured timepoint (AUC0-72hr)?
Participants will be asked to consume three formulations of CoQ10 and will be evaluated for CoQ10 levels in blood, over a 71-day period.
Conditions
- Pharmacokinetic Parameters
- Bioavailability Heathy Volunteers
Interventions
- DIETARY_SUPPLEMENT
-
VitaDry-Q10
Participants consuming a capsule product will be required to consume 2 x 50mg capsules for a combined dose of 100mg with a cup of water.
- DIETARY_SUPPLEMENT
-
VitaSperse-Q10
Participants consuming liquid product will be required to drink a cup of water following administration of 5 mL of study product delivered via syringe.
- DIETARY_SUPPLEMENT
-
Coenzyme Q10
Participants consuming a capsule product will be required to consume 2 x 50mg capsules for a combined dose of 100mg with a cup of water.
Sponsors & Collaborators
-
KGK Science Inc.
collaborator INDUSTRY -
3i Solutions
lead INDUSTRY
Study Design
- Allocation
- RANDOMIZED
- Purpose
- OTHER
- Masking
- QUADRUPLE
- Model
- CROSSOVER
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-03-31
- Primary Completion
- 2026-06-30
- Completion
- 2026-06-30
Countries
- Canada
Study Locations
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