drugset / Trial / NCT01280240

Pharmacokinetic Study of Iron Isomaltoside 1000 Administered by 250 mg IV Bolus Injection or 500 mg Intravenous Infusion to Patients With Non-hematological Malignancies Associated With Chemotherapy Induced Anaemia

NCT01280240

Phase 1 Completed 11 enrolled Pharmacosmos A/S
RandomizedParallel-groupOpen-labelBasic science

Summary

The purpose of this study is to assess Pharmakokinetic properties of iron isomaltoside 1000 (Monofer®) in doses of 250 mg and 500 mg in patients suffering from Chemotherapy Induced anemia.

Timeline

Start
2012-03
Primary completion
2012-09
Completion
2012-11

Drugs

EvaluationDrugModalityDoseRoute
Comparator Iron isomaltoside 1000 Unknown 250 mg Intravenous
Comparator Iron isomaltoside 1000 Unknown 500 mg Intravenous