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Completed Phase 1 Interventional

A Study Comparing the Effects of Epoetin Hospira and Epogen/Epoetin Alfa (Amgen) When Administered IV in Patients With Chronic Renal Failure Requiring Hemodialysis and Receiving Epoetin Maintenance Treatment

ClinicalTrials.gov ID: NCT01170078

Public ClinicalTrials.gov record NCT01170078. 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 29, 2026, 2:53 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

A Phase 1 Study Comparing the Pharmacokinetics of Epoetin Hospira and Epoetin Alfa (Amgen) When Administered Intravenously in Patients With Chronic Renal Failure Requiring Hemodialysis and Receiving Epoetin Maintenance Treatment

Brief summary

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

This study assessed the comparability of the pharmacokinetics (PK) of epoetin following intravenous administration of Hospira Epoetin and Epogen/Epoetin Alfa (Amgen) in patients with chronic renal failure receiving hemodialysis treatment.

Study identification

NCT ID
NCT01170078
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Enrollment
107 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 75 Years
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
Jul 2010 (Type not available)
Primary completion
Jan 2011 (Actual)
Completion
Jan 2011 (Actual)
Last update posted
Mar 20, 2017

2010 – 2011

United States locations

U.S. sites
20
U.S. states
14
U.S. cities
18
Facility City State ZIP Site status
Not listed Downey California 90241 —
Not listed Tarzana California 91356-6123 —
Not listed Denver Colorado 80230 —
Not listed Middlebury Connecticut 06762 —
Not listed Lauderdale Lakes Florida 33313 —
Not listed Miami Florida 33150 —
Not listed Miami Florida 33173 —
Not listed Gurnee Illinois 60031 —
Not listed Wichita Kansas 67214 —
Not listed Detroit Michigan 48236 —
Not listed Pontiac Michigan 48341 —
Not listed Minneapolis Minnesota 55404 —
Not listed Gulfport Mississippi 39501 —
Not listed Philadelphia Pennsylvania 19106 —
Not listed Columbia South Carolina 29203 —
Not listed Knoxville Tennessee 37923 —
Not listed Houston Texas 77054 —
Not listed Houston Texas 77099 —
Not listed San Antonio Texas 78229 —
Not listed Alexandria Virginia 22306 —

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 NCT01170078, 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 Mar 20, 2017 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01170078 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →