Bioavailability Evaluation of curQ+ Curcumin Formulation

Status Enrolling by invitation

Clinical Trial Summary

Clinical Trial Description

This study is intended to evaluate how significantly a proprietary curcumin formulation (curQ+®) results in greater bioavailability compared to 95% curcumin extract over a 6-hour time period following a single oral dose in healthy men & women. Bioavailability will be based upon producing the greatest plasma curcumin concentration (AUC). Secondarily, this study is intended to evaluate the safety and tolerability of the curQ+® curcumin formulation. ;

Study Design

Related Conditions & MeSH terms

Bioavailability

Clinical Trial Details

NCT number	NCT06177483
Study type	Interventional
Source	ESM Technologies, LLC
Contact
Status	Enrolling by invitation
Phase	N/A
Start date	February 25, 2024
Completion date	June 30, 2024

View Details

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