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
| Type | Name | Description |
|---|---|---|
| DRUG | Vicadrostat | Vicadrostat |
| DRUG | Jardiance® | 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.