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A Study of the Safety and Efficacy of Fabrazyme in Patients With Fabry Disease

Phase 3
Completed
Conditions
Fabry Disease
Registration Number
NCT00074971
Lead Sponsor
Genzyme, a Sanofi Company
Brief Summary

People with Fabry disease have an alteration in their genetic material (DNA) which causes a deficiency of the a-galactosidase A enzyme. Fabrazyme 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 ("globatriaosylceramide" 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.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
58
Inclusion Criteria
  • Patients must have successfully completed the previous double-blind study (AGAL-1-002-98)
  • Patients must provide written informed consent prior to study participation
  • Female patients must have a negative pregnancy test prior to each dosing and use a medically accepted method of contraception throughout the study

Exclusion criteria:

  • Patient has undergone kidney transplant or is currently on dialysis
  • Patient is pregnant or lactating
  • Patient is unwilling to comply with the requirements of the protocol
  • Patient has a clinically significant organic disease (with the exception of symptoms related to Fabry disease), including clinically significant cardiovascular, hepatic, pulmonary, neurologic, or renal disease, or other medical condition, serious intercurrent illness, or extenuating circumstances that, in the opinion of the investigator, would preclude participation in the study
Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Morphologic assessment of GL-3 inclusions in the capillary endothelium (vasculature) of the kidney
Safety and efficacy
Secondary Outcome Measures
NameTimeMethod
Changes in McGill Pain Questionnaire
Autonomic status
Glomerular filtration
Functional assessment of urinary protein excretion Ophthalmic changes
SF-36 Health Survey
Physician's assessment of Fabry Symptoms and pain medication

Trial Locations

Locations (20)

Cedars-Sinai Medical Center

🇺🇸

Los Angeles, California, United States

University of California San Fransisco

🇺🇸

San Francisco, California, United States

Northwest Oncology & Hematology Associates

🇺🇸

Coral Springs, Florida, United States

Children's Memorial Hospital

🇺🇸

Chicago, Illinois, United States

University of Iowa Hospital and Clinics

🇺🇸

Iowa City, Iowa, United States

Greater Baltimore Medical Center

🇺🇸

Baltimore, Maryland, United States

Beth Israel Deaconess Medical Center

🇺🇸

Boston, Massachusetts, United States

Fetal Diagnostic and Imaging Center

🇺🇸

Billings, Montana, United States

University of New Mexico

🇺🇸

Albuquerque, New Mexico, United States

Mount Sinai School of Medicine

🇺🇸

New York, New York, United States

Scroll for more (10 remaining)
Cedars-Sinai Medical Center
🇺🇸Los Angeles, California, United States

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