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Terminated Phase 3 Interventional Results available

A Study Comparing Mircera and Epoetin Alfa for the Treatment of Anemia in Dialysis Patients With Chronic Kidney Disease.

ClinicalTrials.gov ID: NCT00422513

Public ClinicalTrials.gov record NCT00422513. 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, 8:22 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 Randomized, Open-label Study Comparing the Pharmacoeconomic (Time and Motion) Benefit of Mircera and Epoetin Alfa in Patients With Chronic Kidney Disease (Stage V) on Dialysis.

Brief summary

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

This 2 arm study will compare 'time and motion' (provider time spent on anemia management) and effect on hemoglobin (Hb) levels, of methoxy polyethylene glycol-epoetin beta (Mircera) and epoetin alfa, in anemic patients with chronic kidney disease (CKD) on hemodialysis. Patients stable on intravenous (iv) epoetin alfa will be randomized either to receive standard of care therapy (epoetin alfa (iv) 3 times weekly), or to receive Mircera 120-360 micrograms (iv), monthly. After a titration period, average time spent on anemia treatment over a 3 month period will be evaluated. The anticipated time on study treatment is 3-12 months, and the target sample size is 100-500 individuals.

Study identification

NCT ID
NCT00422513
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
260 participants

Conditions and interventions

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
Mar 2007 (Type not available)
Primary completion
Dec 2007 (Actual)
Completion
Dec 2007 (Actual)
Last update posted
Dec 14, 2011

2007

United States locations

U.S. sites
44
U.S. states
19
U.S. cities
44
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Rainbow City Alabama — —
Not listed Hot Springs Arizona — —
Not listed Fairfield California — —
Not listed Los Alamitos California — —
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Not listed Mountain View California — —
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Not listed Simi Valley California — —
Not listed Whittier California — —
Not listed Lakewood Colorado — —
Not listed Brandon Florida — —
Not listed Hudson Florida — —
Not listed Lauderdale Lakes Florida — —
Not listed Miami Florida — —
Not listed Ocala Florida — —
Not listed Palm Beach Gardens Florida — —
Not listed Augusta Georgia — —
Not listed Gurnee Illinois — —
Not listed Fort Wayne Indiana — —
Not listed Detroit Michigan — —
Not listed Pontiac Michigan — —
Not listed Sparks Nevada — —
Not listed New Brunswick New Jersey — —
Not listed Brooklyn New York — —
Not listed Brooklyn Center New York — —
Not listed Flushing New York — —
Not listed Orchard Park New York — —
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Not listed Williamsville New York — —
Not listed Raleigh North Carolina — —
Not listed Toledo Ohio — —
Not listed Tulsa Oklahoma — —
Not listed Lancaster Pennsylvania — —
Not listed Lewistown Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed West Homestead Pennsylvania — —
Not listed Columbia South Carolina — —
Not listed Orangeburg South Carolina — —
Not listed Corpus Christi Texas — —
Not listed Houston Texas — —
Not listed Chesapeake Virginia — —
Not listed Fairfax Virginia — —

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 NCT00422513, 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 Dec 14, 2011 · 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 NCT00422513 live on ClinicalTrials.gov.

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