drugset / Trial / NCT00628043

Clinical Study of Epoetin Beta to Chemotherapy-Induced Anemia (CIA) Patients

NCT00628043

Phase 3 Completed 160 enrolled Chugai Pharmaceutical
RandomizedParallel-groupTriple-blindTreatment

Summary

This is a study to investigate the clinical efficacy and safety of epoetin beta 36,000 IU compared with placebo when administrated subcutaneously (s.c.) once-weekly for 12 weeks to anemic patients with lung cancer or gynecologic cancer undergoing chemotherapy.

Timeline

Start
2008-05
Primary completion
2009-05
Completion
2009-09

Drugs

EvaluationDrugModalityDoseRoute
Subject epoetin alfa Protein / enzyme biologic 36000 iu Subcutaneous

Indications