A Web-based Study of Quality of Life Benefits Associated Aranesp in Anemic Patients With Cancer

PHASE4CompletedINTERVENTIONAL
Enrollment

43

Participants

Timeline

Start Date

October 31, 2003

Primary Completion Date

August 17, 2007

Study Completion Date

August 17, 2007

Conditions
AnemiaCancer
Interventions
BIOLOGICAL

darbepoetin alfa

The allocation to the treatment arms will be dependent on the schedule of chemotherapy (i.e. weekly, every 2 week, or every 4 week chemotherapy schedules will receive a starting dose of 200 mcg darbepoetin alfa and every 3 week chemotherapy schedule will receive a starting dose of 300 mcg). Non-responders are defined as patients who experience \<1.0 g/dL increase in hemoglobin concentrations after 6 weeks. Darbepoetin alfa will be held for hemoglobin concentrations \>13.0 g/dL.

Trial Locations (1)

03756

Norris Cotton Cancer Center, Lebanon

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Amgen

INDUSTRY

lead

Dartmouth-Hitchcock Medical Center

OTHER