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Clinical Trial Summary

This study seeks to determine the short-term effects of daily oral supplementation with a new micellar Glutathione formulation (LipoMicel) on the oral absorption and safety of glutathione in healthy volunteers. The primary objective of this study is to evaluate and compare the pharmacokinetics of a novel micellar Glutathione (GSH) formulation with that of a standard formulation as well as a liposomal GSH formulation. The secondary objective is to evaluate the safety of a new micellar GSH formulation with higher bioavailability in human participants over a 30-day study period.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT06345950
Study type Interventional
Source Factors Group of Nutritional Companies Inc.
Contact
Status Completed
Phase N/A
Start date June 21, 2022
Completion date June 30, 2023

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