drugset / Trial / NCT03421002

Determination of Levels of Micafungin in Neonates Suffering From Systemic Candidiasis and/or Candida Meningitis

NCT03421002

NaSingle-groupOpen-labelTreatment

Summary

The primary purpose of this study is to evaluate the pharmacokinetic profile of micafungin administered to neonates suffering from systemic candidiasis. This study will also evaluate the proportion of success and of failure of the therapy with micafungin among treated neonates and will identify a conversion factor to relate plasma levels of micafungin into capillary and venous blood measured through blood samples from the heel and from a peripheral vein, collected simultaneously. Safety of micafungin in neonates will also be assessed.

Timeline

Start
2015-05-30
Primary completion
2018-04-10
Completion
2018-04-10

Drugs

EvaluationDrugModalityDoseRoute
Subject Micafungin Peptide 8 mg/kg Intravenous