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NOT YET RECRUITING
NCT07771166
NA

Effects of N-Acyl Taurines on Incretin Levels in Healthy Subjects

Sponsor: University Hospital, Gentofte, Copenhagen

View on ClinicalTrials.gov

Summary

This study is an investigator-initiated, randomised, double-blind, placebo-controlled, cross-over human trial investigating the effect of arachidonoyl-taurine (C20:4-taurine) and oleoyl-taurine (C18:1-taurine) on GLP-1 secretion during fasting and feeding.

Official title: Effects of N-Acyl Taurines on Incretin Levels in Healthy Subjects: a Randomised, Double-blind, Placebo-controlled, Cross-over Study

Key Details

Gender

All

Age Range

18 Years - 45 Years

Study Type

INTERVENTIONAL

Enrollment

18

Start Date

2027-06

Completion Date

2028-12

Last Updated

2026-08-18

Healthy Volunteers

Yes

Interventions

OTHER

Placebo: First dose at 0 hours

Vehicle (ultrapure water with 10 % fish sauce), orally administered

OTHER

Arachidonoyl-taurine: First dose at 0 hours

Arachidonoyl-taurine (2 mg/kg) dissolved in ultrapure water with 10 % fish sauce, orally administered

OTHER

Oleoyl-taurine: First dose at 0 hours

Oleoyl-taurine (2 mg/kg) dissolved in ultrapure water with 10 % fish sauce, orally administered

OTHER

Liquid meal and second dose of placebo at 3 hours

Liquid meal with 1.5 g paracetamol. Administered with a second dose of: Vehicle (ultrapure water with 10 % fish sauce), orally administered

OTHER

Liquid meal and second dose of OLE-T at 3 hours

Liquid meal with 1.5 g paracetamol. Administered with a second dose of: Oleoyl-taurine (2 mg/kg) dissolved in ultrapure water with 10 % fish sauce, orally administered

OTHER

Liquid meal and second dose of ARA-T at 3 hours

Liquid meal with 1.5 g paracetamol. Administered with a second dose of: Arachidonoyl-taurine (2 mg/kg) dissolved in ultrapure water with 10 % fish sauce, orally administered