Bioavailability of Three Mitopure Formulations

Status Not yet recruiting

Clinical Trial Summary

This study's design as an open-label, single-dose, randomized trial that aligns with the objective of characterizing the concentration-time profiles of three Urolithin A (Mitopure) formulations in a controlled setting. The inclusion criteria, stringent fasting requirements, standardized fluid intake and strict dietary restriction protocols ensure homogeneity among the study participants, enhancing the reliability of the outcomes. Ultimately, this clinical trial aims to contribute valuable insights into the pharmacokinetic behavior of the different Urolithin A formulations, facilitating informed decisions for future developments and applications in the realm of health and wellness.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Healthy Adults

Clinical Trial Details

NCT number	NCT06362018
Study type	Interventional
Source	Amazentis SA
Contact	Dr Gayatri Ganu, MD
Phone	+918554912644
Email	clinical@mprex.in
Status	Not yet recruiting
Phase	N/A
Start date	April 9, 2024
Completion date	June 30, 2024

View Details

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