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NCT06151171

Pharmacokinetics of Different CoQ10 Formulations

Completed NA Last updated 5 December 2023
What this trial tests

NA trial testing CoQ10 in Coenzyme Q10 Pharmacokinetics in 15 participants. Completed in 31 October 2022.

Timeline
1 March 2022
Primary endpoint
31 October 2022
31 October 2022

Quick facts

Lead sponsorFactors Group of Nutritional Companies Inc.
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingdouble
Primary purposetreatment
Enrollment15
Start date1 March 2022
Primary completion31 October 2022
Estimated completion31 October 2022
Sites1 location across Canada

Drugs / interventions tested

Conditions studied

Sponsor

Factors Group of Nutritional Companies Inc. — full company profile →

Who can join

Adults 21 to 65, any sex, with Coenzyme Q10 Pharmacokinetics. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this trial is to compare the bioavailability (AUC, Tmax, and Cmax) of different Coenzyme Q10 preparations in healthy adults. Pharmacokinetic parameters of orally ingested CoQ10 such as AUC, Cmax and Tmax, as well as the ratio of reduced CoQ10 levels to total CoQ10 plasma levels (using the AUC) after administration are compared.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of CoQ10

Trials testing the same drug.

Other Factors Group of Nutritional Companies Inc. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06151171.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing