Overview

Relative Bioavailability Study With Enalapril in Healthy Volunteers

Status:
Unknown status
Trial end date:
2014-10-01
Target enrollment:
Participant gender:
Summary
Phase I study in healthy adult male and female volunteers to compare the bioavailability of enalapril administered in orodispersible Minitablets with or without water in comparison to the standard galenic tablet formulation of enalapril. The standard pharmacokinetic parameters will be calculated from the bioanalytical results for enalapril and enalaprilat and compared in a descriptive statistical analysis.
Phase:
Phase 1
Details
Lead Sponsor:
Ethicare GmbH
Collaborator:
European Commission
Treatments:
Enalapril
Enalaprilat