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Terminated Phase 4 Interventional Results available

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

ClinicalTrials.gov ID: NCT01737879

Public ClinicalTrials.gov record NCT01737879. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 12:00 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

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

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this study is to evaluate whether hemodialysis patients on peginesatide can be converted to epoetin alfa by using a predefined conversion table while achieving a stable hemoglobin.

Study identification

NCT ID
NCT01737879
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 4
Lead sponsor
Amgen
Industry
Enrollment
41 participants

Conditions and interventions

Conditions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Oct 2012 (Type not available)
Primary completion
Mar 2013 (Actual)
Completion
Jul 2013 (Actual)
Last update posted
Apr 21, 2014

2012 – 2013

United States locations

U.S. sites
23
U.S. states
13
U.S. cities
23
Facility City State ZIP Site status
Research Site Phoenix Arizona 85004 —
Research Site Tempe Arizona 85284 —
Research Site Azusa California 91702 —
Research Site Bakersfield California 93309 —
Research Site Granada Hills California 91344 —
Research Site Los Angeles California 90057 —
Research Site Lynwood California 90262 —
Research Site Paramount California 90723 —
Research Site Riverside California 92501 —
Research Site Whittier California 90603 —
Research Site Orange Connecticut 06477 —
Research Site Meridian Idaho 83642 —
Research Site Kansas City Missouri 64111 —
Research Site Bayonne New Jersey 07002 —
Research Site Amherst New York 14221 —
Research Site Yonkers New York 10704 —
Research Site Winston-Salem North Carolina 27103 —
Research Site Oklahoma City Oklahoma 73116 —
Research Site Orangeburg South Carolina 29118 —
Research Site Dyersburg Tennessee 38024 —
Research Site Jackson Tennessee 38305 —
Research Site Houston Texas 77004 —
Research Site Chesapeake Virginia 23320 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01737879, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Apr 21, 2014 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01737879 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →