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Completed Phase 4 Interventional Results available

A Study of the Safety and Efficacy of Fabrazyme (Agalsidase Beta) as Compared to Placebo in Patients With Advanced Fabry Disease

ClinicalTrials.gov ID: NCT00074984

Public ClinicalTrials.gov record NCT00074984. 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 Sep 2, 2026, 10:13 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

Multi-Center, Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Efficacy of Fabrazyme on Progression of Renal Disease and Significant Clinical Events in Patients With Fabry Disease

Brief summary

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

People with Fabry disease have an alteration in their genetic material (DNA) which causes a deficiency of the a-galactosidase A enzyme. Fabrazyme (agalsidase beta) is a drug that helps to breakdown and remove certain types of fatty substances called "glycolipids." These glycolipids are normally present within the body in most cells. In Fabry disease, glycolipids build up in various tissues such as the liver, kidney, skin, and blood vessels because a-galactosidase A is not present, or is present in small quantities. The build up of glycolipid ("globotriaosylceramide" or "GL-3") levels in these tissues in particular is thought to cause the clinical symptoms that are common to Fabry disease. This study will test the safety and efficacy of Fabrazyme in the treatment of patients with Fabry disease.

Study identification

NCT ID
NCT00074984
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Genzyme, a Sanofi Company
Industry
Enrollment
82 participants

Conditions and interventions

Conditions

Interventions

Biological

Eligibility (public fields only)

Age range
16 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
Jan 31, 2001
Primary completion
Dec 31, 2003
Completion
Dec 31, 2003
Last update posted
Dec 26, 2013

2001 – 2004

United States locations

U.S. sites
19
U.S. states
15
U.S. cities
19
Facility City State ZIP Site status
University of Alabama at Birmingham Birmingham Alabama 35294
Cedars-Sinai Medical Center Los Angeles California 90048
University of San Francisco San Francisco California 94143
University of Connecticut Health Partners Farmington Connecticut 06119
Oncology Hematology Association Coral Springs Florida 33065
Emory University School of Medicine Atlanta Georgia 30322
Children's Memorial Hospital Chicago Illinois 60614
University of Kansas Medical Center Kansas City Kansas 66160
Massachusetts General Hospital Boston Massachusetts 02114
Gene Therapy Center - Dept. of Pediatrics and Institute of Human Genetics Minneapolis Minnesota 55455
Children's Hospital Buffalo New York 14209
Mount Sinai School of Medicine New York New York 10029
University of Rochester School of Medicine Rochester New York 14642
Duke University Medical Center Durham North Carolina 27710
Children's Hospital Medical Center Cincinnati Ohio 45229
Children's Hospital of Philadelphia Philadelphia Pennsylvania 19104
University of Pittsburgh Pittsburgh Pennsylvania 15261
Baylor College of Medicine Houston Texas 77030
University of Washington School of Medicine Seattle Washington 98195

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 7 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00074984, 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 26, 2013 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00074984 live on ClinicalTrials.gov.

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