Overview

Long-term PK and Safety/Tolerability Testing LDLL600 Against Esmolol in Healthy Volunteers

Status:
Completed
Trial end date:
2013-01-01
Target enrollment:
Participant gender:
Summary
The study will compare the pharmacokinetics (PK), safety and tolerability of long-term infusion of lyophilized landiolol (LDLL600) against esmolol (Brevibloc) by measurement of blood concentrations of landiolol, esmolol and their metabolites, and by monitoring systemic cardiovascular and local tolerability, blood pressure (BP), ECG including heart rate (HR) and adverse events (AEs).
Phase:
Phase 1
Details
Lead Sponsor:
AOP Orphan Pharmaceuticals AG
Treatments:
Esmolol
Landiolol