drugset / Trial / NCT00272662

Study of Subcutaneously Administered Peginesatide in Anemic Cancer Patients Receiving Chemotherapy

NCT00272662

Phase 2 Completed 60 enrolled Affymax
Non-randomizedParallel-groupOpen-labelTreatment

Summary

The purpose of this study is to evaluate the safety, pharmacodynamics (PD), and pharmacokinetics (PK) of multiple subcutaneously administered injections of peginesatide in anemic cancer participants receiving chemotherapy.

Timeline

Start
2006-01
Primary completion
2007-06
Completion
2007-06

Drugs

EvaluationDrugModalityDoseRoute
Subject peginesatide Peptide 0.05 mg/kg Subcutaneous
Subject peginesatide Peptide 0.1 mg/kg Subcutaneous
Subject peginesatide Peptide 0.15 mg/kg Subcutaneous
Subject peginesatide Peptide 0.2 mg/kg Subcutaneous