drugset / Trial / NCT01249820

Pharmacokinetics of Anidulafungin (Ecalta ®) Intravenous Given to Patients at High Risk for Developing Invasive Fungal Disease

NCT01249820

Phase 2 Completed 26 enrolled Radboud University Medical Center
Non-randomizedSingle-groupOpen-labelOther

Summary

The purpose of this study is to study the pharmacokinetics of anidulafungin (Ecalta ®) given intravenously as antifungal prophylaxis to recipients of an allogeneic haematopoietic stem cell transplant following myeloablative chemotherapy or patients receiving intensive chemotherapy for AML-MDS who are at high risk for developing invasive fungal disease.

Timeline

Start
2010-11
Primary completion
2013-01
Completion
2013-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Anidulafungin Other / unclassified 200 mg Intravenous
Subject Anidulafungin Other / unclassified 300 mg Intravenous