Summary

Location
at UC Davis UC Irvine UCLA UCSD UCSF
Dates
study started
completion around

Description

Summary

The Fabry Registry is an ongoing, international multi-center, strictly observational program that tracks the routine clinical outcomes for patients with Fabry disease, irrespective of treatment status. No experimental intervention is involved; patients in the Registry undergo clinical assessments and receive care as determined by the patient's treating physician.

The primary objectives of the Registry are:

  • To enhance the understanding of the variability, progression, and natural history of Fabry disease, including heterozygous females with the disease;
  • To assist the Fabry medical community with the development of recommendations for monitoring patients and reports on patient outcomes to help optimize patient care;
  • To characterize and describe the Fabry population as a whole;
  • To evaluate the long-term safety and effectiveness of Fabrazyme®

Fabry Pregnancy Sub-registry: This Sub-registry is a multicenter, international, longitudinal, observational, and voluntary program designed to track pregnancy outcomes for any pregnant woman enrolled in the Fabry Registry, regardless of whether she is receiving disease-specific therapy (such as enzyme replacement therapy with agalsidase beta) and irrespective of the commercial product with which she may be treated. Data from the Sub-registry are also used to fulfill various global regulatory requirements, to support product development/reimbursement, and for other research and non-research-related purposes. No experimental intervention is given; thus a patient will undergo clinical assessments and receive standard of care treatment as determined by the patient's physician. If a patient consents to this Sub-registry, information about the patient's medical and obstetric history, pregnancy, and birth will be collected, and, if a patient consents to data collection for her infant, data on infant growth through month 36 postpartum will be collected.

Official Title

Fabry Disease Registry Protocol

Keywords

Fabry Disease, alpha Galactosidase A, aGAL (alpha-galactosidase), Fabry, GL3 (globotriaosylceramide), Anderson-Fabry Disease, angiokeratomas, GLA deficiency (gene deficiency), errors in metabolism

Eligibility

You can join if…

  • Fabry Registry: All patients with a confirmed diagnosis of Fabry disease who have signed the informed consent and patient authorization form(s) are eligible for inclusion. Confirmed diagnosis is defined as a documented deficiency in plasma or leukocyte αGAL (alpha-galactosidase) enzyme activity and/or mutation(s) in the gene coding for αGAL.
  • Fabry Pregnancy Sub-registry:
    • Eligible women must:
      • be enrolled in the Fabry Registry.
      • be pregnant, or have been pregnant with appropriate medical documentation available.
      • provide a signed informed consent and authorization form(s) to participate in the Sub-Registry prior to any Sub-Registry-related data collection being performed.

You CAN'T join if...

Fabry Registry: There are no exclusion criteria. Fabry Pregnancy Sub-registry: There are no exclusion criteria.

Locations

  • University of California at Irvine- Site Number : 840036 accepting new patients
    Irvine California 92697 United States
  • UCLA School Of Medicine- Site Number : 840088 accepting new patients
    Los Angeles California 90095 United States
  • Children's Hospital Oakland- Site Number : 840029 completed
    Oakland California 94609 United States
  • UC Davis MIND Institute- Site Number : 840010 accepting new patients
    Sacramento California 95817 United States
  • University of California at San Diego- Site Number : 840007 completed
    San Diego California 92093 United States
  • University of California at San Francisco- Site Number : 840051 accepting new patients
    San Francisco California United States
  • Southern California Permanente Medical Group- Site Number : 840108 accepting new patients
    Los Angeles California 90027 United States
  • Children's Hospital of Orange County- Site Number : 840074 accepting new patients
    Orange California 92868 United States
  • USC Health Sciences Center Dept of Genetics- Site Number : 840082 accepting new patients
    Los Angeles California 90033 United States
  • Kaiser Permanente Hospital- Site Number : 840042 completed
    Sacramento California 95825 United States

Details

Status
accepting new patients
Start Date
Completion Date
(estimated)
Sponsor
Genzyme, a Sanofi Company
ID
NCT00196742
Study Type
Observational [Patient Registry]
Participants
Expecting 9000 study participants
Last Updated