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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


NCT number NCT06362018
Study type Interventional
Source Amazentis SA
Contact Dr Gayatri Ganu, MD
Phone +918554912644
Email clinical@mprex.in
Status Recruiting
Phase N/A
Start date May 7, 2024
Completion date July 31, 2024

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