Evaluation of the Conversion From Peginesatide to Epoetin Alfa in Patients Receiving Hemodialysis

PHASE4TerminatedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

October 31, 2012

Primary Completion Date

March 31, 2013

Study Completion Date

July 31, 2013

Conditions
Anemia
Interventions
DRUG

Peginesatide

All participants will receive peginesatide for the first 24 weeks.

DRUG

Epoetin alfa

All participants converted to epoetin alfa at week 25 for a total of 32 weeks

Trial Locations (23)

10704

Research Site, Yonkers

14221

Research Site, Amherst

23320

Research Site, Chesapeake

27103

Research Site, Winston-Salem

29118

Research Site, Orangeburg

38024

Research Site, Dyersburg

38305

Research Site, Jackson

64111

Research Site, Kansas City

73116

Research Site, Oklahoma City

77004

Research Site, Houston

83642

Research Site, Meridian

85004

Research Site, Phoenix

85284

Research Site, Tempe

90057

Research Site, Los Angeles

90262

Research Site, Lynwood

90603

Research Site, Whittier

90723

Research Site, Paramount

91344

Research Site, Granada Hills

91702

Research Site, Azusa

92501

Research Site, Riverside

93309

Research Site, Bakersfield

06477

Research Site, Orange

07002

Research Site, Bayonne

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Amgen

INDUSTRY

NCT01737879 - Evaluation of the Conversion From Peginesatide to Epoetin Alfa in Patients Receiving Hemodialysis | Biotech Hunter | Biotech Hunter