drugset / Trial / NCT00989092

Darbepoetin Alfa and Anemia of Cancer

NCT00989092

Phase 2 Terminated 287 enrolled Amgen
RandomizedParallel-groupOpen-labelSupportive care

Summary

This phase 2, multicenter, randomized, open-label, comparative study was designed to determine the effect of darbepoetin alfa on hospital days, economic outcomes, and health related quality of life (HRQOL) in anemic patients with nonmyeloid malignancies who were not receiving chemotherapy. Participants were randomly assigned in a 4:1 allocation ratio to receive either 21 weeks of darbepoetin alfa treatment (treatment group) or 12 weeks of observation followed by up to 9 weeks of darbepoetin alfa treatment (observation group).

Timeline

Start
2002-05
Primary completion
2004-01
Completion
2004-06

Drugs

EvaluationDrugModalityDoseRoute
Subject Darbepoetin alfa Protein / enzyme biologic 3 ug/kg Subcutaneous