CTRI/2018/03/012268
Recruiting
未知
Genzyme rare disease registries (Fabry Disease Registry Protocol)
Sanofi Synthelabo India Private Limited0 sites0 target enrollmentTBD
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Health Condition 1: null- Fabry DiseaseHealth Condition 2: E752- Other sphingolipidosis
- Sponsor
- Sanofi Synthelabo India Private Limited
- Status
- Recruiting
- Last Updated
- 4 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\. all age group from new born to old age allowed.
- •2\. All patients with a confirmed diagnosis of Fabry disease who are willing and able to provide written informed consent and any additional authorization documents required by local law to send health information to the Registry are eligible for inclusion, regardless of whether they are receiving disease therapy including enzyme replacement therapy (ERT) (such as agalsidase beta) and irrespective of the commercial product with which they are being treated.
- •3\. A confirmed diagnosis is defined as a documented deficiency in plasma or leukocyte αGAL enzyme activity and/or mutation(s) in the gene coding for αGA
Exclusion Criteria
- •No exclusion criteria, its a disease registry
Outcomes
Primary Outcomes
Not specified
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