Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Terminated Phase 3 Interventional Results available

A Study of Mircera in Hemoglobin Control of Patients Transitioning to Dialysis.

ClinicalTrials.gov ID: NCT00454246

Public ClinicalTrials.gov record NCT00454246. 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 26, 2026, 2:49 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 of the Effect of Intravenous Mircera on Hemoglobin Control in Patients Transitioning From Chronic Kidney Disease Stage 4 Through Dialysis

Brief summary

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

This study will assess the efficacy and safety of methoxy polyethylene glycol-epoetin beta (Mircera) in the maintenance of hemoglobin levels in patients who have previously received treatment with epoetin alfa or darbepoetin alfa, and who are transitioning from chronic kidney disease stage 4 through dialysis. Patients will be randomized either to receive Mircera or to remain on their existing therapy; the initial monthly dose of subcutaneous (sc) Mircera (120-360 micrograms) will be based on the average weekly dose of epoetin alfa or darbepoetin alfa administered in the week preceding the switch to Mircera. At the initiation of dialysis, patients in the Mircera group will receive monthly intravenous (iv) Mircera at a starting dose based on their previous (sc) dose, and those in the control group will receive weekly (iv) epoetin alfa. The anticipated time on study treatment is 1-2 years, and the target sample size is 500+ individuals.

Study identification

NCT ID
NCT00454246
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
111 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
Apr 2007 (Type not available)
Primary completion
Feb 2008 (Actual)
Completion
Feb 2008 (Actual)
Last update posted
Dec 16, 2011

2007 – 2008

United States locations

U.S. sites
78
U.S. states
32
U.S. cities
78
Facility City State ZIP Site status
Not listed Birmingham Alabama — —
Not listed Mobile Alabama — —
Not listed Phoenix Arizona — —
Not listed El Dorado Arkansas — —
Not listed Hot Springs Arkansas — —
Not listed Bakersfield California — —
Not listed Glendale California — —
Not listed Granada Hills California 91344 —
Not listed Los Angeles California — —
Not listed Orange California — —
Not listed Palm Springs California — —
Not listed Riverside California — —
Not listed San Diego California — —
Not listed Yuba City California — —
Not listed Colorado Springs Colorado — —
Not listed Lakewood Colorado — —
Not listed Stamford Connecticut — —
Not listed Miami Florida — —
Not listed Ocala Florida — —
Not listed Orlando Florida — —
Not listed Palm Beach Gardens Florida — —
Not listed Pembroke Pines Florida — —
Not listed Tampa Florida — —
Not listed Atlanta Georgia — —
Not listed Augusta Georgia — —
Not listed Macon Georgia — —
Not listed Meridan Idaho 83642 —
Not listed Evergreen Park Illinois — —
Not listed Fort Wayne Indiana — —
Not listed Wichita Kansas — —
Not listed Baton Rouge Louisiana — —
Not listed Shreveport Louisiana — —
Not listed Germantown Maryland — —
Not listed Boston Massachusetts — —
Not listed Springfield Massachusetts — —
Not listed Detroit Michigan — —
Not listed Milwaukee Michigan — —
Not listed Royal Oak Michigan — —
Not listed Columbus Mississippi — —
Not listed St Louis Missouri — —
Not listed Omaha Nebraska — —
Not listed Voorhees Township New Jersey — —
Not listed West Orange New Jersey 07052 —
Not listed Brooklyn New York — —
Not listed Buffalo New York — —
Not listed Flushing New York — —
Not listed Great Neck New York — —
Not listed Mineola New York — —
Not listed Springfield Gardens New York — —
Not listed Syracuse New York — —
Not listed The Bronx New York — —
Not listed Durham North Carolina — —
Not listed Greenville North Carolina — —
Not listed Raleigh North Carolina — —
Not listed Winston-Salem North Carolina — —
Not listed Maimisburg Ohio — —
Not listed Toledo Ohio — —
Not listed Portland Oregon — —
Not listed Erie Pennsylvania — —
Not listed Lewistown Pennsylvania — —
Not listed Philadelphia Pennsylvania — —
Not listed Pittsburgh Pennsylvania — —
Not listed Providence Rhode Island — —
Not listed Columbia South Carolina — —
Not listed Greenville South Carolina — —
Not listed Orangeburg South Carolina — —
Not listed Chattanooga Tennessee — —
Not listed Dyersburg Tennessee — —
Not listed Houston Texas 77024 —
Not listed San Antonio Texas — —
Not listed Temple Texas — —
Not listed Alexandria Virginia — —
Not listed Fairfax Virginia — —
Not listed Richmond Virginia — —
Not listed Salem Virginia — —
Not listed Bluefield West Virginia — —
Not listed Morgantown West Virginia — —
Not listed Appleton Wisconsin — —

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 NCT00454246, 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 16, 2011 · Synced Oct 26, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00454246 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →