drugset / Trial / NCT00145652

Adjuvant I.V. Iron Therapy During Erythropoetin Treatment of Anemic Patients With Lymphoproliferative Disorders.

NCT00145652

Phase 3 Completed 66 enrolled Sundsvall Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

This is a multi-center open label, randomized phase-3 study with stratification according to diagnosis and baseline serum-EPO level. The correction of mild or moderate anemia and the effect on iron kinetics by the rHuEPO treatment with or without intravenous iron supplementation in anemic patients with LPD not receiving antineoplastic therapy will be studied. The study will be performed according to the ICH-GCP guidelines. In order to be eligible, the patient must consent in writing that he/she agrees to participate in the study. The patient recruitment period is estimated to be no longer than 18 months.

Timeline

Start
2003-12
Primary completion
Completion
2005-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Iron sucrose Unknown 100 mg Intravenous
Subject epoetin alfa Protein / enzyme biologic 30000 iu Subcutaneous
Subject epoetin alfa Protein / enzyme biologic 60000 iu Subcutaneous