Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT07313436

Extended Release Protein Dosing

VitaKey Extended Release Protein Dosing

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
21 (estimated)
Sponsor
VitaKey Inc. · Industry
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Accepted

Summary

The overall goal of this study is to determine the minimum dose required to elicit measurable elevation of plasma essential amino acid levels 12 hours after consuming VitaKey's extended release protein technology. The results of this study will be used to set a dose for future protein clinical studies.

Conditions

Interventions

TypeNameDescription
OTHERExtended release nutritional proteinParticipants will consume a beverage with extended release protein.
OTHERControlParticipants will consume a beverage with standard nutritional protein.
OTHERNegative DoseParticipants will consume a beverage with 15g less extended release protein than either the low dose cohort or the high dose cohort.

Timeline

Start date
2025-11-17
Primary completion
2026-04-01
Completion
2026-04-01
First posted
2026-01-02
Last updated
2026-03-24

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT07313436. Inclusion in this directory is not an endorsement.