Darbepoetin Alfa MDS Companion Protocol

PHASE3CompletedINTERVENTIONAL
Enrollment

9

Participants

Timeline

Start Date

June 12, 2014

Primary Completion Date

March 20, 2017

Study Completion Date

March 20, 2017

Conditions
Myelodysplastic Syndrome (MDS)
Interventions
DRUG

Darbepoetin Alfa

The first dose of darbepoetin alfa was the same as that administered at the last dosing visit of the active treatment period in Study 20090160. Doses could be increased up to a maximum of 500 μg every two weeks (Q2W).

Trial Locations (4)

3000

Research Site, Leuven

4000

Research Site, Liège

6000

Research Site, Charleroi

9100

Research Site, Sint-Niklaas

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY

NCT02175277 - Darbepoetin Alfa MDS Companion Protocol | Biotech Hunter | Biotech Hunter