drugset / Trial / NCT01308541

A Study to Characterize Pharmacokinetics (PK) and Pharmacodynamics (PD) of LUSEDRA® Administered as Continuous Infusion or Bolus Compared With Continuous Infusion of Propofol Injectable Emulsion

NCT01308541

Phase 1 Completed 20 enrolled Eisai Inc.
RandomizedCrossoverOpen-labelTreatment

Summary

The purpose of this study is to explore the pharmacokinetics (PK) and pharmacodynamics (PD) of LUSEDRA® administered as a continuous infusion or bolus compared with continuous infusion of propofol injectable emulsion.

Timeline

Start
2011-01
Primary completion
2011-08
Completion
2011-08

Drugs

EvaluationDrugModalityDoseRoute
Comparator Propofol Small molecule 14 mg/kg Intravenous
Comparator fospropofol Small molecule 42 mg/kg Intravenous

Indications

No indication recorded.