Safety, Tolerability, and Biosignature of Humanized Prebiotics in Healthy Adults

NACompletedINTERVENTIONAL
Enrollment

63

Participants

Timeline

Start Date

June 13, 2024

Primary Completion Date

March 26, 2025

Study Completion Date

March 26, 2025

Conditions
Intestinal Health
Interventions
DIETARY_SUPPLEMENT

"Humanized galacto-oligosaccharides (hGOS)"

10-15 g/day of hGOS, which will be provided to participants as a powder that can be added to any non-alcoholic beverage

DIETARY_SUPPLEMENT

Galacto-oligosaccharides (GOS)

10-15 g/day of GOS, which will be provided to participants as a powder that can be added to any non-alcoholic beverage.

OTHER

Matching Placebo

10-15 g/day powdered corn syrup comprised of fructose, glucose, and an inert cellulose material that matches the consistency, color sweetness, and taste of the prebiotics, that can be added to any non-alcoholic beverage.

Trial Locations (1)

27599

UNC-Chapel Hill, Chapel Hill

All Listed Sponsors
collaborator

North Carolina Translational and Clinical Sciences Institute

OTHER

lead

University of North Carolina, Chapel Hill

OTHER

NCT06068894 - Safety, Tolerability, and Biosignature of Humanized Prebiotics in Healthy Adults | Biotech Hunter | Biotech Hunter