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NCT06949592: BIOLEMON

Oral Bioavailability of the Phenolic Compounds in a Melissa Supplement

Completed NA Last updated 15 June 2025
What this trial tests

NA trial testing Placebo in Nutrition, Healthy in 10 participants. Completed in 12 June 2025.

Timeline
30 April 2025
Primary endpoint
12 June 2025
12 June 2025

Quick facts

Lead sponsorFytexia
PhaseNA
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designcrossover
Maskingtriple
Primary purposebasic science
Enrollment10
Start date30 April 2025
Primary completion12 June 2025
Estimated completion12 June 2025
Sites1 location across Spain

Drugs / interventions tested

Conditions studied

Sponsor

Fytexia

Who can join

Adults 18 to 60, any sex, with Nutrition, Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The objective of this study is to identify phenolic compound biomarkers of the intake of a mixture of Melissa officinalis extract, acerola extract and vitamin B5. This will be done through the study of their bioavailability and nutrikinetics by measuring their plasma concentrations and urinary excretion over 24h by means of high-performance liquid chromatography coupled with tandem mass spectrometry (HPLC-MS/MS). The study follows a cross-over, double-blind, randomized and placebo control design on 10 healthy subjects

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 recruiting trials for Nutrition, Healthy

Currently open trials in the same condition.

Other Fytexia 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/NCT06949592.

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