Extension Study to Evaluate Safety and Tolerability of Peginesatide for Long-Term Treatment of Anemia in Participants With CKD

PHASE2TerminatedINTERVENTIONAL
Enrollment

81

Participants

Timeline

Start Date

September 30, 2006

Primary Completion Date

November 30, 2009

Study Completion Date

November 30, 2009

Conditions
Chronic Renal FailureChronic Kidney DiseaseAnemia
Interventions
DRUG

peginesatide

Participants received the same initial peginesatide dose as was administered at the end of the previous peginesatide treatment study (NCT00228449) in which the participant was enrolled. The median first dose at study start was 0.087 milligram per kilogram (mg/kg) with an interquartile range of 0.064 to 0.123 mg/kg. Each participant was to receive peginesatide as an injection administered intravenously once every 4 weeks for approximately 54 months in this trial.

Trial Locations (9)

33028

Research Facility, Pembroke Pines

33313

Research Facility, Lauderdale Lakes

37205

Research Facility, Nashville

44718

Research Facility, Canton

48202

Research Facility, Detroit

71101

Research Facility, Shreveport

71603

Research Facility, Pine Bluff

78215

Research Facility, San Antonio

94041

Research Facility, Mountain View

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Affymax

INDUSTRY

NCT00372489 - Extension Study to Evaluate Safety and Tolerability of Peginesatide for Long-Term Treatment of Anemia in Participants With CKD | Biotech Hunter | Biotech Hunter