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Completed Phase 3 Interventional Results available

A Study of Subcutaneous Mircera for the Treatment of Anemia in Dialysis Patients.

ClinicalTrials.gov ID: NCT00077623

Public ClinicalTrials.gov record NCT00077623. 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 Jul 23, 2026, 9:44 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, Controlled, Open-Label, Multi- Center, Parallel-Group Study to Demonstrate the Efficacy and Safety of RO0503821 When Administered Subcutaneously for the Maintenance Treatment of Anemia in Patients With Chronic Kidney Disease Who Are on Dialysis

Study identification

NCT ID
NCT00077623
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hoffmann-La Roche
Industry
Enrollment
572 participants

Conditions and interventions

Conditions

Interventions

  • epoetin alfa or beta 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
Feb 29, 2004
Primary completion
Aug 31, 2005
Completion
Aug 31, 2005
Last update posted
May 24, 2016

2004 – 2005

United States locations

U.S. sites
17
U.S. states
10
U.S. cities
17
Facility City State ZIP Site status
Not listed Hot Springs Arkansas 71901
Not listed Los Angeles California 90033
Not listed Riverside California 92501
Not listed Sacramento California 95816-5119
Not listed San Jose California 95116-1906
Not listed Boston Massachusetts 02130
Not listed Springfield Massachusetts 01107
Not listed Detroit Michigan 48202-2689
Not listed Brooklyn Center Minnesota 55430
Not listed Raleigh North Carolina 27609
Not listed Winston-Salem North Carolina 27157-1023
Not listed Toledo Ohio 43606
Not listed Portland Oregon 97210
Not listed Dallas Texas 75216
Not listed Houston Texas 77030
Not listed San Antonio Texas 78229
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 73 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00077623, 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 May 24, 2016 · Synced Jul 23, 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 protocol, eligibility criteria, and contact information for NCT00077623 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →