ClinicalTrials.gov record
Completed Phase 3 Interventional

A Study of Mircera in the Treatment of Anemia in Patients With Chronic Kidney Disease Not on Dialysis

ClinicalTrials.gov ID: NCT00081471

Public ClinicalTrials.gov record NCT00081471. 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 Apr 29, 2026, 9:44 AM 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 Subcutaneous Mircera on Hemoglobin Level/Correction in Non-dialysis Patients With Chronic Kidney Disease

Study identification

NCT ID
NCT00081471
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
324 participants

Conditions and interventions

Conditions

Interventions

  • darbepoetin alfa Drug
  • methoxy polyethylene glycol-epoetin beta [Mircera] Drug

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
May 31, 2004
Primary completion
Jun 30, 2006
Completion
Jun 30, 2006
Last update posted
Nov 1, 2016

2004 – 2006

United States locations

U.S. sites
22
U.S. states
16
U.S. cities
21
Facility City State ZIP Site status
Not listed Los Angeles California 90073
Not listed Mather California 95655
Not listed Stanford California 94305-5114
Not listed Stamford Connecticut 06902
Not listed Bay Pines Florida 33744
Not listed Ocala Florida 34471
Not listed Shreveport Louisiana 71101
Not listed Boston Massachusetts 02135
Not listed Boston Massachusetts 02215
Not listed Detroit Michigan 48236
Not listed Flushing New York 11355
Not listed Cincinnati Ohio 45220
Not listed Portland Oregon 97201-2940
Not listed Allentown Pennsylvania 18103
Not listed Columbia South Carolina 29209
Not listed Nashville Tennessee 37232
Not listed Austin Texas 78705
Not listed Dallas Texas 75216
Not listed Houston Texas 77054
Not listed Burlington Vermont 05401
Not listed Salem Virginia 24153
Not listed Morgantown West Virginia 26506

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

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 76 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00081471, 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 Nov 1, 2016 · Synced Apr 29, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00081471 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →