Clinical Trials Directory

Trials / Completed

CompletedNCT07035457

A Study in Healthy Men to Compare the Amount of Vicadrostat and Empagliflozin in the Blood When Taken Separately and Together

Relative Bioavailability of Single Doses of Vicadrostat and Empagliflozin Administered Alone Compared to Combined Administration to Healthy Male Subjects (an Open Label, Randomised, Three-way Crossover Trial)

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
15 (actual)
Sponsor
Boehringer Ingelheim · Industry
Sex
Male
Age
18 Years – 55 Years
Healthy volunteers
Accepted

Summary

The main objective of this trial is to investigate the relative bioavailability of vicadrostat and empagliflozin when administered in combination or individually.

Conditions

Interventions

TypeNameDescription
DRUGVicadrostatVicadrostat
DRUGJardiance®Jardiance®

Timeline

Start date
2025-07-02
Primary completion
2025-08-07
Completion
2025-08-15
First posted
2025-06-25
Last updated
2025-08-20

Locations

1 site across 1 country: Germany

Source: ClinicalTrials.gov record NCT07035457. Inclusion in this directory is not an endorsement.